Controlled release of biologically active compounds

ABSTRACT

The present invention relates to biodegradable polymers (e.g., polyesters and polyester amides) derived from functionalized biologically active compounds that can provide site specific delivery of bioactive compounds upon biodegradation in a controlled manner.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Application No. 60/968,917,filed Aug. 30, 2007, the disclosure of which is hereby incorporatedherein by reference in its entirety.

FIELD OF THE INVENTION

This invention is based on the discovery of new class of biodegradablepolymers derived from functionalized biologically active compounds thatcan provide site specific delivery of bioactive compounds uponbiodegradation in a controlled manner.

BACKGROUND OF THE INVENTION

Biologically active compounds are well known (e.g., aspirin andcapsaicin) and have been beneficially administered to patients in needthereof for more than a century. One problem that has been associatedwith many biologically active compounds is that they can be difficult todissolve in water or the human body and can also be very difficult topolymerize. Due to the availability and numerous uses of biologicallyactive compounds, it is desirable to enhance their native value by, forexample, providing compounds or combinations of compounds with aspecific controlled degradation profile or range enabling controlledrelease of the biologically active compound over an extended,controllable time range.

Polymers prepared from aromatic compounds such as terephthalic acid,p-aminobenzoic acid, and p-phenylenediamine exhibit excellent physicalproperties, but the polymers are not biodegradable. Polyesters derivedfrom terephthalic acid, such as polyethylene terephthalate (PET),polytrimethylene terephthalate (PTT), and poly(1,4-butyleneterephthalate) (PBT) are used extensively for making fibers and moldingarticles. Some of these are polymers that are used in biomedicalapplications such as non-absorbable surgical sutures, and these polymersare considered to be safe and biocompatible. Unfortunately, thesepolymers are non-absorbable and, therefore, cannot be used as absorbablesutures or as absorbable polymers for the controlled release of drugs.

Due to the availability and numerous uses of the polymers derived fromthese aromatic compounds, it is desirable to enhance their value, forexample, by functionalizing these aromatic compounds and preparingabsorbable polymers therefrom. The resulting absorbable polymers shouldhave a controlled degradation profile or range enabling controlledrelease of drugs over an extended, controllable time range whenphysically admixed with these polymers.

Synthetic absorbable polymers have been used to produce various surgicalproducts such as sutures, implants, prostheses, and the like, forseveral years. Illustrative U.S. patents describing such polymersinclude U.S. Pat. Nos. 3,297,033, 3,044,942, 3,371,069, 3,531,561,3,636,956, Re. 30,170, and 4,052,988.

Polyesters are used routinely by those skilled in the art in variousdrug delivery systems. For example, U.S. Pat. No. 5,942,252 describes amicrocapsule comprising as its biocompatible excipient apoly(lactide-co-glycolide), poly(lactide), poly(glycolide),copolyoxalate, polycaprolactone, poly(lactide-co-caprolactone),poly(esteramide), polyorthoester, poly(p-hydroxybutyric) acid and/orpolyanhydride which is disclosed as being useful in delivering antigensor vaccines into and through mucosally-associated lymphoid tissue.

WO 99/29885 describes a process which is disclosed as being useful fordegrading poly(ester-amides) and poly(ester-urethanes) encapsulatingchemicals, drugs, enzymes, microorganisms and seeds by introducing thepolymer to an aqueous nutrient solution and inoculating the solutionwith a culture containing a selected bacteria.

WO 98/36013 describes aliphatic-aromatic dihydroxy compounds which aredisclosed as being useful as controlled drug delivery systems.

WO 97/39738 describes the preparation of microparticles which aredisclosed as comprising a sustained release ionic conjugate including afree carboxyl group containing biodegradable polymers and a free aminogroup-containing drug.

U.S. Pat. No. 5,264,540 describes aromatic polyanhydrides which aredisclosed as being biocompatible and biodegradable and which areprepared from para-substituted bis-aromatic dicarboxylic acids for useon wound closure devices. However, these compounds exhibit high melt andglass transition temperatures and decreased solubility, thus making themdifficult to process. The disclosed polyanhydrides also comprise radicalor aliphatic bonds that cannot be hydrolyzed by water.

Polyanhydride polymeric matrices have also been described for use inorthopedic and dental applications. For example, U.S. Pat. No. 4,886,870describes an article that is disclosed as being bioerodible and usefulfor prosthesis and implantation that comprises a biocompatible,hydrophobic polyanhydride matrix. U.S. Pat. No. 5,902,599 describespolymer networks which are formed by polymerizing anhydride prepolymersand which are disclosed as being biodegradable and useful in a varietyof dental and orthopedic applications.

It would be desirable to identify methods and compositions foreffectively delivering biologically active compounds in a controlled andmodifiable fashion. The present invention is directed to these, as wellas other important ends.

SUMMARY OF INVENTION

The present invention is based on the discovery of a new class ofbiodegradable polymers, derived from functionalized biologically activecompounds that can provide site-specific delivery of bioactive compoundsupon degradation in a controlled manner. By varying the functionalizingmoiety or combination of moieties, the rate of biodegradation may bevaried over a period of time, for example, from about one month to aboutfour years, and may be selected as desired, depending on the end-use.

In certain preferred embodiments of the invention, the biodegradablepolyesters have the formula III, VI, or XI, or biodegradable polyamideesters have formula VIII or IX, or pharmaceutically acceptable saltsthereof:

(A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III

wherein the polyester of formula III is formed by condensationpolymerization of monomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II

(B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VI

-   -   wherein the polyester of formula IV is formed by condensation        polymerization of monomers of formula IV and V:        R₆(Y²)_(a)—R₅—(X²)_(b)—R₇  IV        H—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V

(C)—[(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(o)—  VIII

-   -   wherein the polyamide ester of formula VIII is formed by        condensation polymerization of monomers of formula Va and VII:        H—(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—H  Va        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

(D)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(p)—  IX

-   -   wherein the polyamide ester of formula IX is formed by        condensation polymerization of monomers of formula I and VII:        H—(X)_(a)—O—R₁—O—(Y)_(b)—H  I        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

(E)[—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—]_(q)—  XIwherein the polyester of formula XI is formed by self condensationpolymerization of a monomer of formula X:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X

wherein:

-   -   m, n, o, p, and q are each independently an integer from about 5        to about 1000;    -   R₁, R₅, R₉, and R₁₃ are each independently the remaining portion        of a biologically active compound;    -   R₂, R₈, and R₁₀ are each independently the remaining portion of        a biologically active compound or non-biologically active        compound;    -   R₃, R₄, R₆, R₇, R₁₁, R₁₂, and R₁₃ are each independently        selected from Cl, F, Br, and I;    -   X, X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y, Y¹, and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24;    -   each a, b, c, and d is independently an integer from about 1 to        about 6;    -   each e is independently an integer from about 1 to about 6; and    -   each f is independently an integer from about 0 to about 6.

The present invention also provides a method of preparing absorbablepolymer compositions comprising one or more functionalized biologicallyactive compounds and a pharmaceutically acceptable carrier.

The present invention also provides a therapeutic method for treating adisease in a mammal comprising administering to a mammal in need of suchtherapy, an effective amount of a polymer of the present invention.

The present invention also provides a method of delivering abiologically active compound to a mammal comprising administering to themammal a biocompatible and biodegradable polymer of the presentinvention, which degrades to release one or more biologically activecompounds.

The present invention also provides a polymer for use in medicaltherapy, as well as the use of a polymer of the present invention forthe manufacture of a medicament useful for the treatment of a disease ina mammal.

The invention also provides processes of functionalizing biologicallyactive compounds and preparation of biologically active polymers withcontrolled degradation profiles.

DETAILED DESCRIPTION OF THE PRESENT INVENTION

As used herein, the term “biologically active compound” refers to anaturally occurring, semi-synthetic, or synthetic agent that provides apharmaceutically, therapeutically and/or physiologically desirableeffect when administered to a mammal (e.g., human). Biologically activecompounds capable of incorporation into polymers of the presentinvention possess at least two functional groups that may each beincorporated into a linkage of the present polymers, for example, anester or amide linkage such that, upon hydrolysis of the polymer, thebiologically active compound is obtained and/or released in atherapeutically effective form. In preferred embodiments, biologicallyactive compounds that may be useful in the present invention have atleast one aryl or heteroaryl ring and at least one hydroxyl (OH),substituted or unsubstituted amino, or carboxylic acid substituent onthe aromatic or heteroaromatic ring, or functional derivatives of suchsubstituents, such as esters, amides, methyl ethers, and/or glycosides,or other derivatives that would be apparent to those skilled in the art,once placed in possession of the present disclosure.

The biologically active compounds may also comprise other functionalgroups (e.g., hydroxyl groups, amine groups, and carboxylic acid groups)that may be used to modify properties of the polymer (e.g. forbranching, cross linking and/or appending other molecules (e.g. anotherbiologically active compound) to the polymer, for changing thesolubility of the polymer, or for effecting the biodistribution of thepolymer). Exemplary therapeutic agents that may be employed as thebiologically active compounds in the polymers of the present inventionmay be found, for example, in: Physicians' Desk Reference, 61^(st) Ed.,2007, Thomson Healthcare Company; USPN Dictionary of USAN andInternational Drug Names, 2000, The United States PharmacopoeiaConvention, Inc., Rockville, Md.; and The Merck Index, 14^(th) Ed.,2007, John Wiley & Sons, the disclosures of each of which are herebyincorporated herein by reference, in their entireties. One skilled inthe art can readily select therapeutic agents that possess the necessaryfunctional groups for incorporation into the polymers of the inventionfrom these sources, once placed in possession of the teachings in thepresent disclosure.

Therapeutic agents that may be incorporated into the monomers, oligomersor polymers of the present invention include, for example, suitablyfunctionalized analgesics or general or local anesthetics,anti-convulsants, anti-diabetic agents, anti-fibrotic agents,anti-infectives, anti-bacterials, anti-fungals, anti-neoplastics,cardioprotective agents, cardiovascular agents, anti-thrombotics,central nervous system stimulants, cholinesterase inhibitors,contraceptives, deodorants, dopamine receptor agonists, erectiledysfunction agents, fertility agents, gastrointestinal agents, goutagents, hormones, immunomodulators, immunosuppressive, migraine agents,non-steroidal anti-inflammatory drugs (NSAIDs), motion sickness agents,muscle relaxants, nucleoside analogs, neurodegenerative agents (e.g.,Parkinson's disease), obesity agents, ophthalmic agents, osteoporosisagents, parasympatholytics, parasympathommetics, anti-anesthetics,prostaglandins, psychotherapeutic agents, respiratory agents, sedatives,hypnotics, skin and mucous membrane agents, smoking cessation agents,sympatholytics, urinary tract agents, vaginal agents, and vasodilators,and the like (see Physicians' Desk Reference, 61^(st) Ed., 2007, ThomsonHealth Care, the disclosures of which are hereby incorporated herein byreference, in their entireties).

Suitable biologically active compounds include, for example, phenoliccompounds. Phenol is the simplest example of a phenolic compound, but inpreferred embodiments, the phenolic compound has two or more hydroxylgroups. Such phenolic compounds in many instances are bioactivesubstances which occur widely in food plants that are eaten regularly bysubstantial numbers of animals and people. These food-plant bioactivephenolic compounds have typically been found to be safe compounds.Included in the definition of biologically active phenolics are highlysubstituted poly-phenols whose structures include condensed rings.

Examples of naturally occurring biologically active phenolics includebergaptol, caffeic acid, capsaicin, coumarin, daidzein,2,5-dihydroxy-benzoic acid, ferulic acid, flavonoids, glycitein(isoflavone), 4-hydroxycinnamic acid, 4-hydroxy-coumarin,isopimpinellin, resveratrol, sinapic acid, vanillic acid, and vanillin,and derivatives thereof.

Capsaicin is a biologically active phenolic that is the active componentof cayenne pepper. Capsaicin is an amide of vanillylamine and C₈ to C₁₃branched fatty acids and may be a powerful pain reliever. In thisregard, topical application of capsaicin stimulates and blocks smallpain fibers by depleting them of the neurotransmitter substance P thatmediates pain impulses. A cream made, for example, from about 0.025% toabout 0.075% capsaicin applied 4 times daily may help peripheralneuropathic pain, post-herpetic neuralgia, trigeminal neuralgia,psoriasis and fibromyalgia. It may also be useful for diabeticneuropathy, cluster headaches, earache, osteo- and rheumatoid arthritis.

Naproxen, paracetanol, acetaminophen and acetylsalicylic acid arebiologically active phenolics that belong to the class of drugs referredto as non-steroidal anti-inflammatory drugs or NSAIDs. It is generallybelieved that NSAIDs provide relief by blocking the action ofprostaglandins, which are hormone-like substances that contribute topain, inflammation, fever and muscle cramps.

Phenolic moieties, both synthetic and naturally occurring, are includedin many drugs. Examples of these medicinals include acenocoumarol,acetarsol, actinoquinol, adrenalone, alibendol, amodiaquine, anethole,balsalazide, bamethan, benserazide, bentiromide, benzarone,benzquinamide, bevantolol, bifluranol, buclosamide, bupheniode,chlorotrianisene, chloroxylenol, cianidanol, cinepazide, cinitapride,cinepazide, cinmetacin, clebopride, clemastine, clioquinol, cyclovalone,cynarine, denopamine, dextroythyroxine, diacerein, dichlorophen,dienestrol, diethylstilbestrol, diflunisal, diiodohydroxyquinoline,dilazep, dilevalol, dimestrol, dimoxyline, diosmin, dithranol,dobutamine, donepezil, dopamine, dopexamine, doxazosin, entacapone,epanolol, epimestrol, epinephrine, estradiol valerate, estriol, estriolsuccinate, estrone, etamivan, etamsylate, ethaverine, ethoxzolamide,ethyl biscoum-acetate, etilefrine, etiroxate, exalamide, exifone,fendosal, fenoldopam mesilate, fenoterol, fenoxedil, fenticlor,flopropione, floredil, fluorescein, folescutol, formo-terol, gallopamil,gentistic acid, glaziovine, glibenclamide, glucametacin, guajacol,halquinol, hexachlorophene, hexestrol, hexobendine, hexoprenaline,hexylresorcinol, hydroxyethyl salicylate, hydroxystilbamidineisethionate, hymecromone, ifenprodil, indomethacin, ipriflavone,isoetarine, isoprenaline, isoxsuprine, itopride hydrochlor-ide,ketobemidone, khellin, labetalol, lactylphenetidin, levodopa.levomepromazine, levorphanol, levothyroxine, mebeverine, medrylamine,mefexamide, mepacrine, mesalazine, mestranol, metaraminol,methocarbamol, methoxamine, methoxsalen, methyldopa, midodrine,mitoxantrone, morclofone, nabumetone, naproxen, nitroxo-line,norfenefrine, normolaxol, octopamine, omeprazole, orciprenaline,oxilofrine, oxitriptan, oxyfedrine, oxypertine, oxyphenbutazone,oxyphenisatin acetate, oxyquinoline, papaverine, paracetanol,parethoxycaine, phenacaine, phenacetin, phenazocine, phenolphthalein,phenprocoumon, phentolamine, phloedrine, picotamide, pimobendan,prenalterol, primaquine, progabide, propanidid, protokylol,proxymetacaine, raloxifene hydrochloride, repaglinide, reproterol,rimiterol, ritodrine, salacetamide, salazosulfapyridine, salbutamol,salicylamide, salicylic acid, salmeterol, salsalate, sildenafil,silibinin, sulmetozin, tamsulosin, terazosin, terbutaline, tetroxoprim,theo-drenaline, tioclomarol, tioxolone, α-tocopherol (vitamin E),tofisopam, tolcapone, tolterodine, tranilast, tretoquinol, triclosan,trimazosin, trimetazidine, trimethobenz-amide, trimethoprim,trimetozine, trimetrexate glucuronate, troxipide, verapamil,vesnarinone, vetrabutine, viloxazine, warfarin, xamoterol.

Other bioactive phenolics include acacetin,4-acetamido-2-methyl-1-naphthol, acet-aminophen, albuterol, allenolicacid, aloe emodin, aloin, β-amino-4-hydroxy-3,5-di-iodohydrocinnamicacid, N-(5-amino-2-hydroxyphenyl)-benzeneacetamide, 4-amino-1-naphthol,3-aminosalicylic acid, 4-aminosalicylic acid, anacardic acid, p-anol,anthragallol, anthralin, anthranol, anthrarobin, anthrarufin, apigenin,apiin, apocynin, aspidinol, aspirin, baptigenin, benzestrol,benzoresorcinol, bisphenol a, bisphenol b, butylated hydroxylanisole,butylated hydroxytoluene, capobenic acid,trans-1-(3′-carboxy-4′-hydroxyphenyl)-2-(2″,5″-dihydroxyphenyl)ethane,catechin, chlorogenic acid, m-chlorophenol, 5-chloro-8-quinolinol,chloroxylenol, chlorquinaldol, chromo-nar, chrysin, cinametic acid,clorophene, coniferyl alcohol, p-coumaric acid, coumes-trol, coumetarol,daphnetin, datiscetin, deoxyepinephrine, 3,5-diiodothyronine,3,5-di-iodotyro sine, dimethophrine, diosmetin, diresorcinol,disoprofol, dopa, dopamine, drosophilin a, efloxate, ellagic acid,embelin, Equol, eriodictyol, esculetin, esculin, ethylnorepinephrine,ethyl vanillin, eugenol, eupatorin, fenadiazole, ferulic acid, fisetin,3-fluoro-4-hydroxyphenylacetic acid, fraxetin, fustin, galangin,gallacetophe-none, gallic acid, gardenins, genistein, gentisyl alcohol,gepefrine, geranylhydroqui-none, [6]-gingerol, gossypol, guaiacol,guaifenesin, harmalol, hematoxylin, hinderin, homoeriodictyol,homogentisic acid, homovanillic acid, hydroxyamphetamine,2-hyd-roxy-5-(2,5-dihydroxybenzylamino)-2-hydroxybenzoic acid,4-hydroxy-3-methoxy-mandelic acid, n-(p-hydroxyphenyl)glycine,hydroxyprocaine, 8-hydroxyquinoline, hypericin, irigenin, isoproterenol,isoquercitrin, isothebaine, kaempferol, liothyronine, luteolin,mangostin, 5,5′-methylenedisalicylic acid, n-methylepinephrine,metyrosine, morin, mycophenolic acid, myricetin, naringenin, nylidrin,orcinol, osalmid, osthole, oxantel, paroxypropione, pentachlorophenol,3-pentadecylcatechol, p-pentyloxy-phenol, phloretin, phloroglucinol,pinosylvine, plumbagin, pyrocatechol, pyrogallol, quercetagetin,quercetin, resacetophenone, rhamnetin, rhein, sakuranetin, salicylalcohol, salicylanilide, 4-salicyloylmorpholine, salsalate, scopoletin,scutellarein, serotonin,(3,4,5-trihydroxyphenyl)methylenepropanedinitrile, thymol, thyropropicacid, thyroxine, tiratricol, tyrosine, vanillic acid, and vanillin.

Examples of biologically active amino compounds include Aceclofenac,Acedia-sulfone, Alminoprofen, Amisulpride, AmLexanox, Amodiaquine,Amosulalol, Amoxicillin, Amsacrine, Anileridine, Azacyclonol, Baccofen,Balsalazide sodium, Benzocaine, Bromopride, Bumetanide, Carprofen,Carvedilol, Carzenide, Cefprozil, Cinitapride, Clebopride, Clenbuterol,Diclofenac, Ethoxzolamide, Flufenamic acid, Furosemide, Iobenzamic acid,Iocetamic acid, Mefenamic acid, Nadoxolol, D-Nor-pseudoephedrine andparacetamol.

Examples of biologically active carboxylic acid compounds includeAcemetacin, Aceclofenac, Acediasulfone, Adipiodone, Alminoprofen,AmLexanox, Anileridine, Baccofen, Balsalazide sodium, Bentiromide,Benzocaine, Bumetanide, Carprofen, Carzenide, Cinmetacin, Clometacin,Cromoglicic acid, Diclofenac, Diflunisal, Eprosartan, Fendosal,Flufenamic acid, Furosemide, Indometacin, Iobenzamic acid, Iocarmicacid, Iocetamic acid, Iodoxamic acid, Ioglycamic acid, Iophenoic acid,Iotroxic acid, Mefenamic acid, Naproxen, Nedocromil, Repaglinide,Salazosulfapyridine, Salicylic Acid, Salsalate, and Sarpogrelate.

Flavonoids, sometimes called bioflavonoids, are 3-ring phenoliccompounds consisting of a double ring attached by a single bond to athird ring. Examples include flavonoids, flavanones, flavones,flavanols, anthocyanidins, proanthocyanidins, procyanidolic oligomers(PCO), catechins, biflavans, polyphenols, rutin, rutinosides,hydroxyethylrutosides (HER), hesperidin, quercetin, quercetrin,polyphenols, catechin, epicatechin, epicatechin gallate,epigallocatechin gallate, and leucoanthocyanins. Flavonoids include thewater-soluble pigments, such as anthocyanins, that are found in cellvacuoles. Flavonols are colorless or yellow flavonoids found in leavesand many flowers.

A therapeutic dose of bioflavonoids is helpful for conditions related toChronic Venous Insufficiency (CVI). Some examples are: thrombophlebitis,thrombosis, varicose veins, leg ulcers, spider veins, hemorrhoids,chronic nosebleeds, prolonged menstrual bleeding. Even eye problems likemacular degeneration and diabetic retinopathy have been helped withbioflavonoids. Along with the anti-inflammatory effects, bioflavonoidscan be very helpful for tendonitis, arthritis, rheumatoid arthritis,joint injury, fibromyalgia, cellulite, and gout. Bioflavonoids,specifically proanthcyanidins, are found in grape seed extract. Theproanthcyanidins appear to enhance the activity of vitiamin C. Thebioflavonoids in grape seed extract may also reduce the painfulinflammation of swollen joints and prevent the oxidation of cholesterolin arteries that leads to plaque in the arterial walls.

Isoflavones exert a broad spectrum of biological activities. Besidesantioxidant and estrogenic activities, isoflavones protect againstseveral chronic diseases. Results of epidemiological studies indicatethat consumption of soybean isoflavones lowers the incidence of breast,prostate, urinary tract and colon cancers. They also provide protectionagainst coronary heart diseases and osteoporosis. Examples ofisoflavones include are glycitein (isoflavone), daidzein, prunetin,biochanin A, orobol, santal, pratensein, formononetin, genistein,glycitein, and the glucosides, β-glycosides and other derivatives of theaforementioned isoflavones.

Further examples of biologically active compounds with hydroxyl,carboxyl and/or amino groups useful in the present invention may befound in the following texts, the disclosures of which are herebyincorporated herein by reference, in their entireties.

-   -   a. Shahidi, Ferriodoon and Marian Naczk, Phenolics in Food and        Nutriceuticals, Boca Raton, Fla.: CRC Press, 2003.    -   b. Kleemann, A. et al, Pharmaceutical Substances, 4th Edition,        Thieme (2000).    -   c. Phenolic Compounds in Food and Their Effects on Health II;        Antioxidants and Cancer Prevention, ACS Symposium Series No.        507, Washington, D.C.: ACS, 1992.    -   d. Food Phytochemicals for Cancer Prevention I, ACS Symposium        Series N. 546, Washington, D.C.: ACS, 1994.    -   e. ROMPP Encyclopedia Natural Products, New York: Thieme, 2000.    -   f. The Merck Index, 14^(th) edition, John Wiley & Sons, 2007.    -   g. A Single Source for Flavonoids and Coumarins (2005-2006),        INDOFINE Chemical Company, Inc. 2006.

The present invention provides novel biodegradable polyesters of formulaIII or a pharmaceutically acceptable salt thereof:—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III

wherein the polyester is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II

wherein:

-   -   m is an integer from about 5 to about 1000;    -   R₁ is the remaining portion of a biologically active compound;    -   R₂ is the remaining portion of a biologically active compound or        non-biologically active compound;    -   R₃ and R₄ are independently selected from Cl, F, Br, and I;    -   X and X¹ are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y and Y¹ are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

The present invention also provides novel biodegradable polyesters offormula VI or a pharmaceutically acceptable salt thereof:—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VI

wherein the polyester is formed by condensation polymerization ofmonomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O′)C—R₈—C(═O)O—(Y¹)_(d)—H  V

wherein:

-   -   n is an integer from about 5 to about 1000;    -   R₅ is the remaining portion of a biologically active compound;    -   R₆ and R₇ are independently selected from Cl, F, Br, and I;    -   R₈ is the remaining portion of a biologically active compound or        non-biologically active compound;    -   X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y¹ and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

The present invention also provides novel biodegradable polyamide estersof formula VIII or a pharmaceutically acceptable salt thereof:—[(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(o)—  VIII

wherein the polyamide ester is formed by condensation polymerization ofmonomers of formula Va and VII:H—(—X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—H  VaR₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

wherein:

-   -   o is an integer from about 5 to about 1000;    -   R₉ is the remaining portion of a biologically active compound;    -   R₁₀ is the remaining portion of a biologically active compound        or non-biologically active compound;    -   R₁₁ and R₁₂ are independently selected from Cl, F, Br, and I;    -   X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y¹ and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

The present invention also provides novel biodegradable polyamide estersof formula IX or a pharmaceutically acceptable salt thereof:—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(p)—  IX

wherein the polyamide ester is formed by condensation polymerization ofmonomers of formula I and VII:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₁₁—(Y²)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

wherein:

-   -   p is an integer from about 5 to about 1000;    -   R₁ is the remaining portion of a biologically active compound;    -   R₁₀ is the remaining portion of a biologically active compound        or non-biologically active compound;    -   R₁₁ and R₁₂ are independently selected from Cl, F, Br, and I;    -   X and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—; and,    -   Y and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

The present invention also provides novel biodegradable polyesters offormula XI or a pharmaceutically acceptable salt thereof:[—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—]_(q)—  XIwherein the polyester is formed by self condensation polymerization of amonomer of formula X:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  Xwherein:

-   -   q is an integer from about 5 to about 1000;    -   R₁₃ is the remaining portion of a biologically active compound;    -   R₁₄ is selected from Cl, F, Br, and I;    -   Y is independently at each occurrence —CH₂C(═O)O— (glycolic acid        moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each e is independently an integer from about 1 to about 6; and    -   each f is independently an integer from about 0 to about 6.

The present invention also provides novel biodegradable monomers offormulas I, II, IV, V, Va, VII, or X, as defined herein.

The groups represented by X, X¹, X², Y, Y¹, and Y² are attached in themonomers, oligomers and polymers of the present invention as shown.Their left hand sides are attached to the variable or H shown in thecorresponding formula to be on the left of the X, X¹, X², Y, Y¹, or Y²group and on their right hand sides to the variable or H shown in thecorresponding formula to be on the right of the X, X¹, X², Y, Y¹, or Y²group.

As set forth in formulas I, II, III, IV, V, VI, VII, VIII, IX, X and XIabove, each of a, b, c, d and e is independently an integer from about 1to about 6 (and all combinations and subcombinations of integer rangesand specific integers therein).

In certain preferred embodiments of the present invention, a is theinteger 1, 2, or 3.

In other embodiments of the present invention, b is the integer 1 or 2.

In still other embodiments of the present invention, c is the integer 1.

As set forth in formulas X and XI above, f is independently an integerfrom about 0 to about 6 (and all combinations and subcombinations ofinteger ranges and specific integers therein).

As set forth in formulas III, VI, VIII and IX above, each of m, n, o, pand q is independently an integer of from about 5 to about 1000 (and allcombinations and subcombinations of integer ranges and specific integerstherein). In some preferred embodiments of the present invention, eachof m, n, o, p and q is independently the integer 5, 10, 20, 30, 40, 50,60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, or 800, or an integerof from 900 to 1,000.

In the above groups X, X¹, X², Y, Y¹ and Y², each y and z isindependently an integer from about 2 to about 24 (and all combinationsand subcombinations of integer ranges and specific integers therein). Incertain preferred embodiments, each y and z is independently selectedfrom the integers 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16,17, 18, 19, 20, 21, 22, 23, or 24.

In certain preferred embodiments of the present invention, X, X¹, and X²are independently at each occurrence selected from: —OC(═O)CH₂—;—OC(═O)CH(CH₃)—; —OC(═O)CH₂CH₂OCH₂—; and —OC(═O)CH₂CH₂CH₂CH₂CH₂—; morepreferably selected from —OC(═O)CH₂— and —OC(═O)CH(CH₃)—.

In other preferred embodiments of the present invention, Y, Y¹, and Y²are independently at each occurrence selected from: —CH₂C(═O)O—;—CH(CH₃)C(═O)O—; —CH₂CH₂OCH₂C(═O)O—; and, —CH₂CH₂CH₂CH₂CH₂C(═O)O—; morepreferably selected from —CH₂C(═O)O— and —CH(CH₃)C(═O)O—.

In certain embodiments of the present invention the biologically activeor non-biologically active compound has one or more amino groups whichare incorporated into the backbone of the polymer of the invention.Whenever a Y, Y¹, or Y² is directly attached through its carboxylterminus (the CO₂ side of the Y, Y¹, or Y²) to an amino group of thebiologically active or non-biologically active compound, the resultingbond is an amide bond. For example, when Y is CH₂—C(═O)O— and thebiologically active compound to which it is attached ispara-aminobenzoic acid, the resultant moiety is para-CH₂—C(═O)NH-benzoicacid. Similarly, whenever an X, X¹, or X² is directly attached throughits carboxyl terminus (the CO₂ side of the X, X¹, or X²) to an aminogroup of the biologically active or non-biologically active compound,the resulting bond is an amide bond.

The polymers of the present invention are designed such that thebackbones comprise at least about one or at least about two functionalgroups that will preferably yield a biologically active form of abiologically active compound upon hydrolysis of the polymer.

The present invention also provides novel therapeutic methods forproducing effects or treating diseases by administering to a patient inneed thereof a therapeutically effective amount of at least one polymerof the present invention. Examples of effects and diseases include ananalgesic effect, cancer, an anti-inflammatory effect. an anti-bacterialeffect, an anti-fungal effect, an immunosuppressive effect, ananti-thrombotic effect, psoriasis, inflammatory bowel disease, skincancer, brain tumor, an anti-infective effect, and pain.

In other preferred embodiments of monomers and/or oligomers of thepresent invention, R³, R⁴, R⁶, R⁷, R¹¹, and R¹² are each independentlyCl, Br, or I, more preferably Cl or Br, with Cl being even morepreferred.

Examples of biologically active compounds that may be included in themonomers, oligomers or polymers of the present invention includephenolic compounds such as phenols, naphthols, indoles, acetophenones,benzophenones, coumarins, furanocoumarins, alkaloids, catechins,chromones, chalcones, flavonoids or bioflavonoids, isoflavones, drugscontaining phenolic groups, and natural products containing phenolicgroups.

Examples of biologically active dihydroxy compounds that may be includedin the monomers, oligomers or polymers of the present invention includeAdrenalone, Alfuzosin, Alibendol, Amrubicin, Apomorphine, Bamethan,Benzquinamide, Bevantolol, Bifluranol, Bisacodyl, Brodimoprim,Bunazosin, Bupheniode, Carbidopa, Carbuterol, Cyclofenil, Cyclovalone,Daunorubicin, Dichlorophen, Dienestrol, Diethylstilbestrol, Dimestrol,Dithranol, Donepezil, Doxefazepam, Doxorubicin, Entacapone, Epinepheine,Epirubicin, Esomeprazole, Etamivan, Etamsylate, Etilefrine, Ezetimibe,Fenticlor, Fluorescein, Folescutol, Formoterol, Gefitinib, Hexestrol,Hexylresorcinol, Hydroxyethyl salicylate, Ifenprodil, Isoetarine,Isoxsuprine, Itopride. HCl, Khellin, Labetalol, Mitoxantrone,Morclofone, Moxaverine, Normolaxol, Omeprazole, Oxilofrine, Oxepertine,Phenacaine, Phenolphthalein, Prazosin, Tolcapone, Vesnarinone, andVetradutine.

Examples of biologically active diamino compound that may be included inthe monomers, oligomers or polymers of the present invention includeAmisulpride, Amodiaquine, Amosulalol, Amoxicillin, Amsacrine,Azacyclonol, Bromopride, Carvedilol, Cefprozil, Cinitapride, Clebopride,Clenbuterol, Ethoxzolamide, Nadoxolol, and D-Norpseudoephedrine.

Examples of biologically active hydroxy/amino compounds that may beincluded in the monomers, oligomers or polymers of the present inventioninclude Amisulpride, Amodiaquine, Amosulalol, Amoxicillin, Amsacrine,Azacyclonol, Bromopride, Carvedilol, Cefprozil, Cinitapride, Clebopride,Clenbuterol, Ethoxzolamide, Nadoxolol, D-Norpseudoephedrine, andparacetamol.

Examples of biologically active dicarboxylic acid compounds that may beincluded in the monomers, oligomers or polymers of the present inventioninclude Adipiodone, Cromoglicic acid, Eprosartan, Iocarmic acid,Iodoxamic acid, Ioglycamic acid, Iotroxic acid, Nedocromil.

Examples of biologically active hydroxy/carboxylic acid compounds thatmay be included in the monomers, oligomers or polymers of the presentinvention include Acemetacin, Bentiromide, Cinmetacin, Clometacin,Diflunisal, Fendosal, Indometacin, lophenoic acid, Naproxen,Repaglinide, Salazosulfapyridine, Salicylic Acid, Salsalate, andSarpogrelate.

Examples of biologically active hydroxyl-acids that may be included inthe monomers, oligomers or polymers of the present invention include4-hydroxycinnamic acid, caffeic acid, chlorogenic acid, ferulic acid,sinapic acid, vanillic acid, Acemetacin, Bentiromide, Cinmetacin,Clometacin, Diflunisal, Fendosal, Indometacin, lophenoic acid, Naproxen,Repaglinide, Salazosulfapyridine, Salicylic Acid, Salsalate, andSarpogrelate.

Examples of biologically active amino/carboxylic acid compounds that maybe included in the monomers, oligomers or polymers of the presentinvention include Aceclofenac, Acediasulfone, Alminoprofen, AmLexanox,Anileridine, Baccofen, Balsalazide sodium, Benzocaine, Bumetanide,Carprofen, Carzenide, Diclofenac, Flufenamic acid, Furosemide,Iobenzamic acid, Iocetamic acid, and Mefenamic acid.

Examples of biologically active diamino compounds that may be includedin the monomers, oligomers or polymers of the present invention includeAmisulpride, Amodiaquine, Amosulalol, Amoxicillin, Amsacrine,Azacyclonol, Bromopride, Carvedilol, Cefprozil, Cinitapride, Clebopride,Clenbuterol, Ethoxzolamide, Nadoxolol, D-Norpseudoephedrine, amino acids(L-lysine), and natural products.

Non-biologically active diol compounds include saturated andunsaturated, substituted and unsubstituted alkyl, aryl and alkylarylgroups having 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or18 carbon atoms. Alternatively, polyalkylene oxides having weightaverage molecular weights of from about 500 to about 5,000 may be usedas a diol (i.e., a polydiol). Suitable diols or polydiols for use in thepresent invention are diol or diol repeating units with up to about 8carbon atoms. Examples of suitable diols include 1,2-ethanediol(ethylene glycol); 1,2-propanediol (propylene glycol); 1,3-propanediol;1,4-butanediol; 1,5-pentanediol; 1,3-cyclopentanediol; 1,6-hexanediol;1,4-cyclohexanediol; 1,8-octanediol; and, combinations thereof. Examplesof polydiols include polyethylene glycol and polypropylene glycol withweight average molecular weights of from about 500 to about 5000.

Examples of non-biologically active dicarboxylic compounds useful in thepresent invention include saturated and unsaturated, substituted andunsubstituted alkyl, aryl and alkylaryl groups having 1, 2, 3, 4, 5, 6,7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or 18 carbon atoms.Alternatively, non biologically active symmetrical and non symmetricaldicarboxylic acids as shown below can also be used in the presentinvention;

Examples of non-biologically active diamino compounds useful in thepresent invention include saturated and unsaturated, substituted andunsubstituted alkyl, aryl and alkylaryl groups having 2, 3, 4, 5, 6, 7,8, 9, 10, 11, 12, 13, 14, 15, 16, 17, or 18 carbon atoms. Alternatively,polyalkylene oxides that are diamines with weight average molecularweights from about 500 to about 5,000 may be used. Alternatively, nonbiologically active symmetrical and non symmetrical diamines as shownbelow can also be used in the present invention;

The definitions and examples provided in this application are notintended to be limiting, unless specifically stated.

“Patient” as used herein refers to any animal in need or medical care orother treatment that employs the polymers of the invention. The termanimal includes for example, mammals, especially those warm bloodedmammals that are typically under medical care (e.g., humans anddomesticated animals). Examples of mammals include feline, canine,equine, bovine, and human, more preferably human.

The monomers and polymers described herein may be useful in medicalapplications, including as drug delivery devices and other medicaldevices. The terms “medical applications” and “medical devices”, as usedherein, encompass medical and biomedical applications and include alltypes of applications involved in the practice of medicine that wouldbenefit from a material that may decompose harmlessly within about aknown or desired period of time. Examples include medical and surgicaldevices, which include drug delivery systems (e.g., a site-specific orsystemic drug delivery systems or matrices), tissue engineering (e.g.,tissue scaffold), stent coatings, stents, porous devices, implantablemedical devices, molded articles (e.g., vascular grafts, stents, boneplates, sutures, implantable sensors, and barriers for surgical adhesionprevention), wound closure devices (e.g., surgical clips, staples, andsutures), coatings (e.g., for endoscopic instruments, sutures, stents,and needles), fibers or filaments (which may be attached to surgicalneedles or fabricated into materials including sutures or ligatures,multifilament yarn, sponges, gauze, tubes, and sheets for typing up andsupporting damaged surface abrasions), rods, films (e.g., adhesionprevention barriers), knitted products, foodstuffs, nutritionalsupplements, nutraceuticals, cosmetics, pharmaceuticals, biodegradablechewing gums, flavors, enhanced drugs, drug intermediates, cancerpreventing agents, antioxidants, controlled release preparations, andsolvents for drugs. Examples of knitted products, woven or non-woven,and molded products include: burn dressings; hernia patches; medicateddressings; facial substitutes; gauze, fabric, sheet, felt, or sponge forliver hemostasis; gauze bandages; arterial graft or substitutes;bandages for skin surfaces; suture knot clip; orthopedic pins, clamps,screws, and plates; clips (e.g., for vena cava); staples; hooks,buttons, and snaps; bone substitutes (e.g., mandible prosthesis);intrauterine devices (e.g., spermicidal devices); draining or testingtubes or capillaries; surgical instruments; vascular implants orsupports; vertebral discs; extracorporeal tubing for kidney andheart-lung machines; and, artificial skin.

The rate of hydrolysis of the materials of the present invention willdepend upon a number of factors, including the functionalization usedand the number of functionalizations present on the at leastdifunctionalized aromatic (e.g., from about 1 to about 6). For example,glycolic acid modified aromatics should generally hydrolyze more quicklythan aromatics modified with dioxanone, whereas lactic acid andcaprolactone modified aromatics should generally hydrolyze over a longerperiod of time as compared to glycolic acid and dioxanone modifiedaromatics. Furthermore, it is expected that the rate of hydrolysis willincrease as the number of functional groups is increased. Thus, desiredtime ranges for hydrolysis and therefore release of biologically activeagents may be obtained by altering the number and type offunctionalization used to functionalize the aromatics.

Polymers of the present invention preferably have weight-averagemolecular weights above about 10,000 including, for example, about20,000 or above, about 30,000 or above, about 40,000 or above, about50,000 or above, about 60,000 or above, about 70,000 or above, about80,000 or above, including about 90,000 to about 100,000 daltons,calculated from gel permeation chromatography (GPC) relative topolystyrene standards in tetrahydrofuran (THF) without furthercorrection.

The polymers of the present invention may preferably be processed byknown methods commonly employed in the field of synthetic polymers toprovide a variety of useful articles with valuable physical and chemicalproperties. The useful articles may be shaped by conventionalpolymer-forming techniques such as extrusion, compression molding,injection molding, solvent casting, and wet spinning. Shaped articlesprepared from the polymers may be useful, for example, as degradabledevices for medical implant applications.

The present invention also relates to compositions, comprising: at leastone functionalized aromatic, wherein the composition is suitable for useas at least one of the following: (a) a solvent for drugs; (b) anutritional compound; (c) a cosmetic: and, (d) a pharmaceutical. Each ofthe compositions may further comprise an additional component suitablefor such compositions. For example, when the composition is suitable foruse as a cosmetic it may further comprise one or more cosmeticingredients. Also, when the composition is suitable for use as apharmaceutical it may further comprise one or more pharmaceuticallyacceptable excipients. In addition, each of the compositions maycomprise a difunctionalized aromatic derived from a aromatic having aproperty useful to that type of composition. For example, the startingaromatic may be (a) a nutritional supplement or a food intermediary; (b)an anticancer agent; (c) an antimicrobial agent; (d) ananti-inflammatory agent; (e) a pain-reducer; and, (f) an antioxidantagent. Also, the compositions may further comprise one of agents(a)-(f).

The compositions of the present invention may be suitable foradministration via a route selected from oral, enteral, parenteral,topical, transdermal, ocular, vitreal, rectal, nasal, pulmonary, andvaginal.

The implantable medical devices of the present invention comprise atleast one absorbable polymer of the present invention. For example, apolymer of the present invention may be combined with a quantity of abiologically active compound sufficient to be therapeutically effectiveas a site-specific or systemic drug delivery system (see Gutowska etal., J. Biomater. Res., 29, 811-21 (1995) and Hoffman, J. ControlledRelease, 6, 297-305 (1987), the disclosures of which are herebyincorporated herein by reference, in their entirety). Another example ofthe present invention is a method for site-specific or systemic drugdelivery by implanting in the body of a patient in need thereof animplantable drug delivery device comprising a therapeutically effectiveamount of a biologically active compound in combination with at leastone absorbable polymer of the present invention.

In another example, at least one polymer of the present invention isformed into a porous device (see Mikos et al., Biomaterials, 14, 323-329(1993) or Schugens et al., J. Biomed. Mater. Res., 30, 449-462 (1996))to allow for the attachment and growth of cells (see Bulletin of theMaterial Research Society, Special Issue on Tissue Engineering (GuestEditor: Joachim Kohn), 21(11), 22-26 (1996)). The disclosures of theforegoing publications are hereby incorporated herein by reference, intheir entireties. Thus, the present invention provides a tissue scaffoldcomprising a porous structure for the attachment and proliferation ofcells either in vitro or in vivo formed from at least one absorbablepolymer of the present invention

The present invention also relates to an article (e.g., an implantablemedical device), comprising a metal or polymeric substrate havingthereon a coating, wherein the coating comprises at least one polymer ofthe present invention.

The present invention also relates to a molded article prepared from atleast one polymer of the present invention.

Controlled release mechanisms are known in the art. See, for example,Langer, R., Science 249: 1527-1533 (1990); WO 02/09768; WO 02/09767; WO01/41753; WO 99/12990, the disclosures of which are hereby incorporationherein by reference, in their entireties. Any and all controlled releasemechanisms and formulations may be employed in practicing the invention,provided it allows for the controlled release of the biologically activecompounds at, or near, the site of interest.

Polymeric drug delivery systems comprising the polymers of the inventionmay be readily processed into pastes or solvent cast to yield films,coatings, nanoparticles e.g. nanospheres, microparticles e.g.microspheres and fibers with different geometric shapes for design ofvarious medical devices, and may also be processed by compressionmolding and extrusion. In one embodiment, a polymer or polymers may becoated onto or applied onto a medical device, such as, e.g., by formingthe polymer or polymers into a covering. In another embodiment, thepolymer or polymers may be formed into a medical device, such as, e.g.,an implant. In one embodiment of the present invention, a polymercomprising a functional group or agent may used to form a covering, suchas, e.g., a coating or a sheath, that partially or completely coversand/or surrounds a medical device. Such a covering may cover a portionof the medical device or it may completely cover a medical device. Thecovering may be divided into separate portions or several smallercoverings may be present on the medical device. In another embodiment ofthe invention, a polymer may surround the medical device, or a portionthereof, and may have the form of a coating, a layer, a film, andcombinations thereof. The polymer may be in the form of a solid or asemi-solid, such as a gel, sheath, a wrap, a tube or a cuff covering allor a portion of the medical device. The polymer may be rigid,semi-rigid, or non-rigid. The coating of polymer may be, for example,about 100 nm, about 1 mm, about 1 mm, or about 1 cm thick, although someporous implants may benefit from longer lasting effects enabled by acoating that completely fills the interstices of the device with, insome cases, a thin coating on those surfaces proximal to bone or othertissue upon placement in the body. In one embodiment, the polymercoating may be comprised of microparticles, such as microspheres thatmay typically but not necessarily be less than about 10 microns indiameter. These microparticles may be applied to the surface of amedical device before placement in the body. A sterile liquid may beused to coat the device to adhere such microspheres for minutes to weeksto enable uncoated medical devices to benefit from the same or similartherapeutic benefits as coated devices.

A polymer, compound and/or composition of the invention may be appliedor coated onto a medical implant by any means known in the artincluding, but not limited to, solvent methods such as, for example,dipping and spray-drying, and non-solvent methods such as chemical vapordeposition, extrusion coating, covalently grafting or dipping in moltenpolymer, compound and/or composition of the invention. The method ofpreparation may vary depending on the polymer, compound and compositionand/or the medical implant. The medical implant may be formed from orcoated with one or more layers of the same or different polymer,compound and/or composition of the invention. In another example, apolymer, compound and/or composition of the invention may be coated ontoa medical implant in the shape of a membrane or tube for use in thetreatment of injury or damage to the peripheral nervous system or ablock of solid or foamed composition containing pathways drilled orotherwise formed to encouraged nerve growth or bone growth. In the aboveinstances, bioerosion of the disc, membrane, tube or block would yieldor generate an agent included within the polymer or composition. Thepolymer may be formed into a device by any means known in the artincluding, but not limited to, molding e.g. compression or blow molding,and extrusion. The medical device may be formed from one or more of thesame or different polymer, compound and/or composition of the invention.A polymer, compound and/or composition of the invention may be formed,that is, physically configured, into various shapes, geometries,structures and configurations including, but not limited to, a film,fiber, rod, coil, corkscrew, hook, cone, pellet, tablet, tube e.g.smooth or fluted, disc, membrane, microparticle, nanoparticle,“biobullet” i.e. bullet shaped, seed i.e. bullet shaped or targetedseeds, as well as those described in the above identified products,patents and articles, including in some cases forming medical implantsthat have the same, similar or completely different functionalcharacteristics compared to those functional characteristics of themedical devices described in the above identified products, patents andarticles. The above-mentioned shapes, geometries, structures andconfigurations may contain additional features that will further enhancethe desired application or use. For example, a polymer, compound and/orcomposition of the invention in the form of a rod, coil, or cone mayhave barbs that spring out upon insertion from a needle or cannula orwhen warmed to body temperature to reduce movement and/or expulsion. Theshape, geometry, structure or configuration of a device, such as amedical implant, will vary depending upon the use of the device. Forexample, for treatment of a spinal cord injury or concussion to thebrain, a polymer, compound and/or composition of the invention may beformed into a medical implant in the shape of a disc for placement underthe dura or dura mater, or a solution, suspension, emulsion, cream, gel,ointment, or other adhesive formulation form for covering the spine,dura or other surgically exposed areas, film, sprayed or coatedformulation. In another example, a polymer, compound and/or compositionof the invention may be formed into a medical implant in the shape of amembrane or tube for use in the treatment of injury or damage to theperipheral nervous system or a block of solid or foamed compositioncontaining pathways drilled or otherwise formed to encourage nervegrowth or bone growth. In another example, in the treatment of cancer, apolymer, compound and/or composition of the invention may be formed intoa medical implant in the shape of a pellet, microparticle e.g.microsphere, nanoparticle e.g. nanosphere, rod, membrane, pin, cuff,disc, bullet, hook, rod or cone, with or without barbs, for insertion ina bone, joint, tumor excision site or other structures, or for insertionwithin the same and other structures. In the above instances, bioerosionof the medical implant would yield or generate an agent.

The present invention also relates to a controlled drug delivery systemcomprising at least one polymer of the present invention physicallyadmixed with a biologically or pharmacologically active agent. Forexample, the controlled drug delivery system can comprise a biologicallyor pharmacologically active agent coated with at least one polymer ofthe present invention.

The present invention also relates to a controlled drug delivery systemcomprising a biologically or pharmacologically active agent physicallyembedded or dispersed into a polymeric matrix formed from at least onepolymer of the present invention.

The present invention also relates to a tissue scaffold having a porousstructure for the attachment and proliferation of cells, either in vitroor in vivo, formed from one least one polymer of the present invention.

The present invention also relates to a composition comprising at leastone polymer of the present invention, which has been further polymerizedwith at least one lactone monomer selected from glycolide, lactide,p-dioxanone, trimethylene carbonate, ether lactones, morpholinediones,and caprolactone.

The present invention also relates to an implantable biomedical devicecomprising at least one polymer that has been further polymerized withat least one lactone monomer.

The present invention also relates to a biodegradable chewing gumcomposition comprising an effective amount of at least one polymer thathas been further polymerized with at least on lactone monomer.

The present invention also relates to an article (e.g., an implantablemedical device) comprising a metal or polymeric substrate and havingthereon a coating, wherein said coating comprises at least one polymerthat has been further polymerized with at least one lactone monomer.

The present invention also relates to a molded article prepared from atleast one polymer that has been further polymerized with at least onelactone monomer.

The present invention also relates to a monofilament or multifilamentprepared from at least one polymer that has been further polymerizedwith at least one lactone monomer.

The present invention also relates to a controlled drug delivery systemcomprising at least one polymer that has been further polymerized withat least one lactone monomer, which has been physically admixed with abiologically or pharmacologically active agent.

The present invention also relates to a controlled drug delivery systemcomprising a biologically or pharmacologically active agent physicallyembedded or dispersed into a polymeric matrix formed from at least onepolymer that has been further polymerized with at least one lactonemonomer.

The present invention also relates to a tissue scaffold having a porousstructure for the attachment and proliferation of cells, either in vitroor in vivo, formed from at least one polymer that has been furtherpolymerized with at least one lactone monomer.

The present invention also relates to low molecular weight polymers oroligomers of the compounds of the present invention that are furtherreacted to form reactive end groups (e.g., isocyanates, expoxides,acrylates and the like). Low-molecular weight polymers or oligomers asused herein means a polymer having a number average molecular weight ofabout 500 to about 20,000 (and all combinations and subcombinations ofranges of number average molecular weights and specific molecularweights therein), with about 500 to about 10,000 being preferred. Forexample, some of the compounds of the present invention may behavechemically like diols. They may therefore be reacted with dicarboxylicacids to form polyesters, which are usually hydroxyterminated. Thesehydroxyterminated oligomers may be further reacted to form, for example,isocyanates, epoxides and acrylates. Similarly the compounds of thepresent invention may be reacted with isocyanates to make urethanes.Thus, the present invention also includes compositions comprising atleast one polymer of the present invention, which has been furtherreacted to form reactive end groups.

The present invention also relates to polymers made from compounds ofthe present invention that have been sterilized, for example, bycobalt-60 radiation, electron beam radiation, and/or ethylene oxide.

“Bioabsorbable” or “absorbable” as used herein means that the materialreadily reacts or enzymatically degrades upon exposure to bodily tissuefor a relatively short period of time, thereby experiencing asignificant weight loss in that short period of time. Completebioabsorption/absorption should take place within about twenty fourmonths, although it may be complete within about nine months or withinabout six months. In this manner, the polymers of the present inventionmay be fabricated into medical and surgical devices, which may be usefulfor a vast array of applications requiring complete absorption within arelatively short time period.

The biological properties of the bioabsorbable polymers of the presentinvention used to form a device or part thereof, as measured by itsabsorption rate and its breaking strength retention in vivo (BSR), maybe varied to suit the needs of the particular application for which thefabricated medical device or component is intended. This can beconveniently accomplished by varying the ratio of components of thepolymer chosen.

“Pharmaceutically acceptable salts” refer to derivatives of thedisclosed compounds wherein the parent compound is modified by makingacid or base salts thereof. Examples of pharmaceutically acceptablesalts include, but are not limited to, mineral or organic acid salts ofbasic residues such as amines; alkali or organic salts of acidicresidues such as carboxylic acids; and the like. The pharmaceuticallyacceptable salts include the conventional non-toxic salts or thequaternary ammonium salts of the parent compound formed, for example,from non-toxic inorganic or organic acids. For example, suchconventional non-toxic salts include, but are not limited to, thosederived from inorganic and organic acids selected from1,2-ethanedisulfonic, 2-acetoxybenzoic, 2-hydroxyethanesulfonic, acetic,ascorbic, benzenesulfonic, benzoic, bicarbonic, carbonic, citric,edetic, ethane disulfonic, ethane sulfonic, fumaric, glucoheptonic,gluconic, glutamic, glycolic, glycollyarsanilic, hexylresorcinic,hydrabamic, hydrobromic, hydrochloric, hydroiodide, hydroxymaleic,hydroxynaphthoic, isethionic, lactic, lactobionic, lauryl sulfonic,maleic, malic, mandelic, methanesulfonic, napsylic, nitric, oxalic,pamoic, pantothenic, phenylacetic, phosphoric, polygalacturonic,propionic, salicyclic, stearic, subacetic, succinic, sulfamic,sulfanilic, sulfuric, tannic, tartaric, and toluenesulfonic.

The pharmaceutically acceptable salts of the present invention can besynthesized from the parent compound that contains a basic or acidicmoiety by conventional chemical methods. Generally, such salts can beprepared by reacting the free acid or base forms of these compounds witha stoichiometric amount of the appropriate base or acid in water or inan organic solvent, or in a mixture of the two; generally, non-aqueousmedia like ether, ethyl acetate, ethanol, isopropanol, or acetonitrileare preferred. Lists of suitable salts are found in Remington'sPharmaceutical Sciences, 18th ed., Mack Publishing Company, Easton, Pa.,1990, p 1445, the disclosure of which is hereby incorporated byreference.

“Therapeutically effective amount” includes an amount of a compound ofthe present invention that is effective when administered alone or incombination to treat the desired indication.

“Alkyl” includes both branched and unbranched saturated aliphatichydrocarbon groups having the specified number of carbon atoms. C₁₋₆alkyl, for example, includes C₁, C₂, C₃, C₄, C₅, and C₆ alkyl groups.Examples of alkyl include methyl, ethyl, n-propyl, i-propyl, n-butyl,s-butyl, t-butyl, n-pentyl, s-pentyl, and n-hexyl.

“Aryl” refers to any stable 6, 7, 8, 9, 10, 11, 12, or 13 memberedmonocyclic, bicyclic, or tricyclic ring, wherein at least one ring, ifmore than one is present, is aromatic. Examples of aryl includefluorenyl, phenyl, naphthyl, indanyl, and tetrahydronaphthyl.

“Heteroaryl” refers to any stable 5, 6, 7, 8, 9, 10, 11, or 12 membered,(unless the number of members is otherwise recited), monocyclic,bicyclic, or tricyclic heterocyclic ring that is aromatic, and whichconsists of carbon atoms and 1, 2, 3, or 4 heteroatoms independentlyselected from the group consisting of N, O, and S. If the heteroaryl isdefined by the number of carbons atoms, then 1, 2, 3, or 4 of the listedcarbon atoms are replaced by a heteroatom. If the heteroaryl group isbicyclic or tricyclic, then at least one of the two or three rings mustcontain a heteroatom, though both or all three may each contain one ormore heteroatoms. If the heteroaryl group is bicyclic or tricyclic, thenonly one of the rings must be aromatic. The N group may be N, NH, orN-substituent, depending on the chosen ring and if substituents arerecited. The nitrogen and sulfur heteroatoms may optionally be oxidized(e.g., S, S(O), S(O)₂, and N—O). The heteroaryl ring may be attached toits pendant group at any heteroatom or carbon atom that results in astable structure. The heteroaryl rings described herein may besubstituted on carbon or on a nitrogen atom if the resulting compound isstable.

Examples of heteroaryl include acridinyl, azocinyl, benzimidazolyl,benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl,benzoxazolinyl, benzthiazolyl, benztriazolyl, benztetrazolyl,benzisoxazolyl, benzisothiazolyl, benzimidazolinyl, carbazolyl,4aH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl,decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl,dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolyl,1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, 3H-indolyl,isatinoyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl,isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, naphthyridinyl,oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl,1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxindolyl, pyrimidinyl,phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl,phenoxathinyl, phenoxazinyl, phthalazinyl, pteridinyl, pyranyl,pyrazinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole,pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, 2H-pyrrolyl, pyrrolyl,quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl,tetrazolyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl,1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl,thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl,thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl,1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, and xanthenyl.

Polymers of the present invention may be made in the form of randomcopolymers or block copolymers. A coupling agent may also be added tothe polymers of the present invention. A coupling agent is a reagentthat has a least two functional groups that are capable of covalentlybonding to two different monomers. Examples of coupling agents includetrifunctional or tetrafunctional polyols, oxycarboxylic acids, andpolybasic carboxylic acids (or acid anhydrides thereof). Other couplingagents include the difunctional groups (e.g., diols, diacids, diamines,and hydroxy-acids) previously discussed. The addition of the couplingagents causes the branching of long chains, which can impart desirableproperties in the molten state to the pre-polymer. Examples ofpolyfunctional coupling agents include trimethylol propane, glycerin,pentaerythritol, malic acid, citric acid, tartaric acid, trimesic acid,propane tricarboxylic acid, cyclopentane tetracarboxylic anhydride, andcombinations thereof.

A “pre-polymer” is a low-molecular weight polymer, as previouslydefined, that have reactive end groups (e.g., hydroxy groups) that canbe further reactive with, for example, the lactone monomers.

The amount of coupling agent to be added before gelation occurs is afunction of the type of coupling agent used and the polymerizationconditions of the polymer or molecular weight of the pre-polymer towhich it is added. Generally in the range of from about 0.1 to about 10mole percent of a trifunctional or a tetrafunctional coupling agent maybe added based on the moles of polymers present or anticipated from thesynthesis.

The polymerization of a polyester of the present invention can beperformed under solution polymerization conditions in the presence of antriethylamine catalyst at room temperature to below about 80° C.,preferably at about room temperatures. The exact reaction conditionschosen will depend on numerous factors, including the properties of thepolymer desired, the viscosity of the reaction mixture, and the glasstransition temperature and softening temperature of the polymer. Desiredreaction conditions of temperature, time and pressure can be readilydetermined by assessing these and other factors. Generally, the reactionmixture will be maintained at about room temperature for many hours. Thepolymerization reaction can be allowed to proceed at this temperatureuntil the desired molecular weight and percent conversion is achievedfor the copolymer, which will typically take about 15 minutes to about40 hours. Increasing the reaction temperature generally decreases thereaction time needed to achieve a particular molecular weight.

Polymerization conditions for the preparation of other types of polymersof the present invention (e.g., polyamides) are described in theliterature. Those skilled in the art will recognize that the polymersdescribed herein can be made from known procedures, once armed with theteachings of the present disclosure.

Copolymers of the absorbable polymers of the present invention can beprepared by preparing a pre-polymer in solution, isolating, purifyingand drying, then adding at least one lactone monomer or lactonepre-polymer. The mixture could then be subjected to the desiredconditions of temperature and time to copolymerize the pre-polymer withthe lactone monomers.

A lactone pre-polymer is a pre-polymer formed by ring openingpolymerization with a known initiator (e.g., ethylene glycol, diethyleneglycol, glycerol, or other diols or triols).

The molecular weight of the pre-polymer as well as its composition canbe varied depending on the desired characteristic, which the pre-polymeris to impart to the copolymer. For example, the pre-polymers of thepresent invention, from which the copolymer is prepared, generally havea molecular weight that provides an inherent viscosity between about 0.2to about 2.0 deciliters per gram (dl/g) as measured in a 0.1 g/dlsolution of hexafluoroisopropanol at 25° C. Those skilled in the artwill recognize that the pre-polymers described herein can also be madefrom mixtures of more than one diol or dicarboxylic acid.

One of the beneficial properties of the polyesters of the presentinvention is that the ester linkages are hydrolytically unstable, andtherefore the polymer is bioabsorbable because it readily breaks downinto small segments when exposed to moist bodily tissue. In this regard,while it is envisioned that co-reactants could be incorporated into thereaction mixture of the dicarboxylic acid and the diol for the formationof the polyester pre-polymer, it is preferable that the reaction mixturedoes not contain a concentration of any co-reactant which would renderthe subsequently prepared polymer non-absorbable. The reaction mixturecan be substantially free of any such co-reactants if the presencethereof results in a non-absorbable polymer.

The polymers of the present invention can be melt processed by numerousmethods to prepare a vast array of useful devices. These polymers can beinjection or compression molded to make implantable medical and surgicaldevices, especially wound closure devices.

Alternatively, the polymers can be extruded to prepare fibers. Thefilaments thus produced may be fabricated into sutures or ligatures,attached to surgical needles, packaged, and sterilized by knowntechniques. The polymers of the present invention may be spun asmultifilament yarn and woven or knitted to form sponges or gauze, (ornon-woven sheets may be prepared) or used in conjunction with othermolded compressive structures as prosthetic devices within the body of ahuman or animal where it is desirable that the structure have hightensile strength and desirable levels of compliance and/or ductility.Examples include tubes, including branched tubes, for artery, vein, orintestinal repair, nerve splicing, tendon splicing, sheets for typing upand supporting damaged surface abrasions, particularly major abrasions,or areas where the skin and underlying tissues are damaged or surgicallyremoved.

Additionally, the polymers can be molded to form films which, whensterilized, are useful as adhesion prevention barriers. Anotheralternative processing technique for the polymers of the presentinvention includes solvent casting, particularly for those applicationswhere a drug delivery matrix is desired.

The polymers of the present invention can be used to coat a surface of asurgical article to enhance the lubricity of the coated surface. Thepolymer may be applied as a coating using conventional techniques. Forexample, the polymer may be solubilized in a dilute solution of avolatile organic solvent (e.g. acetone, methanol, ethyl acetate, ortoluene), and then the article can be immersed in the solution to coatits surface. Once the surface is coated, the surgical article can beremoved from the solution where it can be dried at an elevatedtemperature until the solvent and any residual reactants are removed.

For coating applications, the polymer should exhibit an inherentviscosity, as measured in a 0.1 gram per deciliter (g/dl) ofhexafluoroisopropanol (HFIP), between about 0.05 to about 2.0 dl/g orabout 0.10 to about 0.80 dl/g. If the inherent viscosity were less thanabout 0.05 dl/g, then the polymer may not have the integrity necessaryfor the preparation of films or coatings for the surfaces of varioussurgical and medical articles. On the other hand, it is possible to usepolymers with an inherent viscosity greater than about 2.0 dl/g, thoughit may be difficult to do so.

Numerous surgical articles (including but not limited to endoscopicinstruments) can be coated with the polymer of the present invention toimprove the surface properties of the article. By way of example,specific surgical articles include surgical sutures, stents, andneedles. More specifically the surgical article may be a suture, whichmay be attached to a needle. The suture may also be a syntheticabsorbable suture. These sutures are derived, for example, fromhomopolymers and copolymers of lactone monomers such as glycolide,lactide, ε-caprolactone, 1,4-dioxanone, and trimethylene carbonate. Thesuture can be a braided multifilament suture composed of polyglycolideor poly(glycolide-co-lactide).

The amount of coating polymer to be applied on the surface of a braidedsuture can be readily determined empirically, and will depend on theparticular copolymer and suture chosen. Ideally, the amount of coatingcopolymer applied to the surface of the suture may range from about 0.5to about 30 percent of the weight of the coated suture or from about 1.0to about 20 weight percent, or from about 1 to about 5 percent byweight. If the amount of coating on the suture were greater than about30 weight percent, then it may increase the risk that the coating mayflake off when the suture is passed through tissue

Sutures coated with the polymers of the present invention are desirablebecause they have a more slippery feel, thus making it easier for thesurgeon to slide a knot down the suture to the site of surgical trauma.In addition, the suture is more pliable, and therefore is easier for thesurgeon to manipulate during use. These advantages are exhibited incomparison to sutures which do not have their surfaces coated with thepolymer of the present invention.

When the article of the present invention is a metal stent, the amountof coating applied to the surface of the article is an amount whichcreates a layer with a thickness ranging, for example, between about 2to about 20 microns on the stent or about 4 to about 8 microns. If theamount of coating on the stent were such that the thickness of thecoating layer was greater than about 20 microns, or if the thickness wasless than about 2 microns, then the desired performance of the stent asit is passed through tissue may not be achieved.

When the article of the present invention is a surgical needle, theamount of coating applied to the surface of the article is an amountwhich creates a layer with a thickness ranging, for example, from about2 to about 20 microns on the needle, preferably of about 4 to about 8microns. While coatings outside this range may still be operable, theperformance of the needle as it is passed through tissue may not beoptimum.

The polymers of the present invention can also be used as apharmaceutical carrier in a drug delivery matrix. To form this matrixthe polymer can be mixed with a therapeutic agent to form the matrix.There are a variety of different therapeutic agents, which can be usedin conjunction with the polymers of the invention. In general,therapeutic agents which may be administered via the pharmaceuticalcompositions of the invention include, antiinfectives such asantibiotics and antiviral agents; analgesics and analgesic combinations;anorexics; antihelmintics; antiarthritics; antiasthmatic agents;anticonvulsants; antidepressants; antidiuretic agents; antidiarrheals;antihistamines; antiinflammatory agents; antimigraine preparations;antinauseants; antineoplastics; antiparkinsonism drugs; antipruritics;antipsychotics; antipyretics, antispasmodics; anticholinergics;sympathomimetics; xanthine derivatives; cardiovascular preparationsincluding calcium channel blockers and beta-blockers such as pindololand antiarrhythmics; antihypertensives; diuretics; vasodilatorsincluding general coronary, peripheral and cerebral; central nervoussystem stimulants; cough and cold preparations, including decongestants;hormones such as estradiol and other steroids, includingcorticosteroids; hypnotics; immunosuppressives; muscle relaxants;parasympatholytics; psychostimulants; sedatives; and tranquilizers; andnaturally derived or genetically engineered proteins, polysaccharides,glycoproteins, or lipoproteins.

The drug delivery matrix may be administered in any suitable dosage formincluding orally, parenterally, subcutaneously as an implant, vaginally,or as a suppository. Matrix formulations containing the polymers of thepresent invention may be formulated by mixing one or more therapeuticagents with the polymer. The therapeutic agent, may be present as aliquid, a finely divided solid, or any other appropriate physical form.Typically, but optionally, the matrix will include one or moreadditives, e.g., nontoxic auxiliary substances such as diluents,carriers, excipients, or stabilizers. Other suitable additives may beformulated with the polymers of the present invention andpharmaceutically active agent. If water is to be used, then it can beuseful to add it just before administration.

The amount of therapeutic agent will be dependent upon the particulardrug employed and medical condition being treated. Typically, the amountof drug represents about 0.001% to about 70%, about 0.001% to about 50%,or about 0.001% to about 20% by weight of the matrix.

The quantity and type of polymer incorporated into a composition (e.g.,parenterally delivered composition) will vary depending on the releaseprofile desired and the amount of drug employed. The product may containblends of polymers of the present invention to provide the desiredrelease profile or consistency to a given formulation.

The polymers of the present invention, upon contact with body fluidsincluding blood or the like, undergoes gradual degradation (mainlythrough hydrolysis) with concomitant release of the dispersed drug for asustained or extended period (as compared to the release from anisotonic saline solution). This can result in prolonged delivery (e.g.,over about 1 to about 2,000 hours or about 2 to about 800 hours) ofeffective amounts (e.g., about 0.0001 mg/kg/hour to about 10 mg/kg/hour)of the drug. This dosage form can be administered as is necessarydepending on the subject being treated, the severity of the affliction,and the judgment of the prescribing physician.

Individual formulations of drugs and polymers of the present inventionmay be tested in appropriate in vitro and in vivo models to achieve thedesired drug release profiles. For example, a drug could be formulatedwith a polymer of the present invention and orally administered to ananimal. The drug release profile could then be monitored by appropriatemeans such as, by taking blood samples at specific times and assayingthe samples for drug concentration. Following this or similarprocedures, those skilled in the art will be able to formulate a varietyof formulations.

The polymers of the present invention can have controllable hydrolysisprofiles, improved bioavailability, improved efficacy and enhancedfunctionality. The difunctional compounds can readily polymerize intobiodegradable polyesters, polyester amides, for example, useful for manyapplications, including biomedical applications, foodstuffs, nutritionalsupplements, cosmetics, medicaments, coatings and others readilyapparent to one skilled in the art.

An aspect of this invention is to combine these molecules, such asglycolic acid, lactic acid, p-dioxanone, ε-caprolactone, —(CH₂)_(y)COO—,where y is one of the integers 2, 3, 4 and from 6 to 24, and—(CH₂CH₂O)_(z) CH₂COO—, where z is an integer from 2 to 24, witharomatic compound, to form a new chemical entity. Preferential examplesof functionalization molecules are glycolic acid, lactic acid,p-dioxanone, and ε-caprolactone. This functionalization enhances thenative value of the aromatic compound by releasing the aromatic moietyby hydrolysis or degradation of the compound. The compound may degradeunder controllable conditions in the environment, in the body of ananimal, for example a mammal, including a human.

The glycolic acid moiety, lactic acid moiety, dioxanone moiety,caprolactone moiety, moieties of —(CH₂)_(y)COO— where y is one of theintegers 2, 3, 4 and from 6 to 24, and moieties of —(CH₂CH₂O)_(z)CH₂COO—where z is an integer from 2 to 24, have different hydrolysis ordegradation rates and times over which they release the active aromaticmoiety and thus do the difunctionalized aromatic acid made from them.The species used for functionalization supplies the release time orrange dictated by the application. Glycolic acid based compoundshydrolyze faster than p-dioxanone based whereas lactic acid andcaprolactone based compounds take much longer to hydrolyze than glycolicacid and p-dioxanone based compounds. This desired time range may beobtained by using a combination of difunctionalized aromatic compounds,that is, a blend of two or more functionalized compounds made from anytwo or more of the species glycolide, lactide, dioxanone andpolydioxanone combined with one aromatic compound.

The array of difunctionalized compounds developed as an aspect of theinvention, have a wide range of hydrolysis rates that are controllable.The specific moiety or combination of moieties used forfunctionalization yields a compound or mixture with specific hydrolysisranges.

Bioactive Formulations

In other aspects of the present invention some polymers of the presentinvention can be further manufactured into formulations suitable fororal, rectal, parenteral (for example, subcutaneous, intramuscular,intradermal, or intravenous), transdermal, vitreal or topicaladministration. The most suitable route in any given case will depend onthe nature and severity of the condition being treated and on the natureof the particular active compound that is being used. The formulationsof a pharmaceutical composition are typically admixed with one or morepharmaceutically or veterinarially acceptable carriers and/or excipientsas are well known in the art.

Formulations suitable for oral administration may be presented indiscrete units, such as capsules, cachets, lozenges, or tablets, eachcontaining a predetermined amount of the active compound; as a powder orgranules; as a solution or a suspension in an aqueous or non-aqueousliquid; or as an oil-in-water or water-in-oil emulsion.

Compositions of the present invention suitable for parenteraladministration conveniently comprise sterile aqueous preparations of theactive compounds, which preparations are preferably isotonic with theblood of the intended recipient.

Formulations suitable for rectal administration are preferably presentedas unit dose suppositories.

Formulations suitable for ocular or vitreal administration may bepresented as bioabsorbable coatings for implantable medical devices,injectables, liquids, gels or suspensions.

Formulations or compositions suitable for topical administration to theskin preferably take the form of an ointment, cream, lotion, paste, gel,spray, aerosol, or oil. Examples of carriers that conventionally usedinclude Vaseline, lanoline, polyethylene glycols, alcohols, andcombination of two or more thereof.

Formulations suitable for transdermal administration may be presented asdiscrete patches adapted to remain in intimate contact with theepidermis of the recipient for a prolonged period of time.

The active compounds may be provided in the form of foodstuffs ornutrition supplements, such as being added to, admixed into, coated,combined or otherwise added to a foodstuff. The term foodstuff is usedin its widest possible sense and includes liquid formulations such asdrinks including dairy products, biodegradable chewing gums, and otherfoods, such as health bars, desserts, etc. Food formulations containingcompounds of the invention can be readily prepared according to standardpractices.

Compounds of the formula used as medicaments or pharmaceuticals aretypically administered in a manner and amount as is conventionallypracticed. See, for example, Goodman and Gilman, The PharmaceuticalBasis of Therapeutics, current edition, the disclosures of which arehereby incorporated herein by reference, in their entireties.

Compounds of the present invention may have potent antioxidant activityand increased acidity of their aromatic component, as well as theimproved biodegradation provided by the functionalization, and thus findwide application in pharmaceutical and veterinary uses, in cosmeticssuch as more effective skin creams to prevent skin ageing, in sunscreens, in foods, health drinks, nutritional supplements, shampoos, andthe like.

Dosages

Useful dosages of the polymers can be determined by comparing their invitro activity, and in vivo activity of the therapeutic agent in animalmodels. Methods for the extrapolation of effective dosages in mice, andother animals, to humans are known in the art; see, for example, U.S.Pat. No. 4,938,949, the disclosures of which are hereby incorporatedherein by reference, in their entireties. Additionally, useful dosagescan be determined by measuring the rate of hydrolysis for a givenpolymer under various physiological conditions. The amount of a polymerrequired for use in treatment will vary not only with the particularpolymer selected but also with the route of administration, the natureof the condition being treated and the age and condition of the patientand will be ultimately at the discretion of the attendant physician orclinician.

The desired dose may conveniently be presented in a single dose or asdivided doses administered at appropriate intervals, for example, astwo, three, four or more sub-doses per day. The sub-dose itself may befurther divided, e.g., into a number of discrete loosely spacedadministrations.

Combination Therapies

The polymers of the invention are also useful for administering acombination of therapeutic agents to an animal. Such a combinationtherapy can be carried out, for example, in the following ways: (1) asecond therapeutic agent can be dispersed within the polymer matrix of apolymer of the invention, and can be released upon degradation of thepolymer; (2) a second therapeutic agent can be appended to a polymer ofthe invention (i.e. not in the backbone of the polymer) with bonds thathydrolyze to release the second therapeutic agent under physiologicalconditions; (3) the polymer of the invention can be incorporated withtwo therapeutic agents into the polymer backbone (e.g. a polymercomprising one or more units of formula (II)) or (4) two polymers of theinvention, each with a different therapeutic agent can be administeredtogether (or within a short period of time).

Thus, the invention also provides a pharmaceutical compositioncomprising a polymer of the invention and a second therapeutic agentthat is dispersed within the polymer matrix of a polymer of theinvention. The invention also provides a pharmaceutical compositioncomprising a polymer of the invention having a second therapeutic agentappended to the polymer (e.g. with bonds that will hydrolyze to releasethe second therapeutic agent under physiological conditions).

The polymers of the invention can also be administered in combinationwith other therapeutic agents that are effective to treat a givencondition to provide a combination therapy. Thus, the invention alsoprovides a method for treating a disease in a mammal comprisingadministering an effective amount of a combination of a polymer of theinvention and another therapeutic agent. The invention also provides apharmaceutical composition comprising a polymer of the invention,another therapeutic agent, and a pharmaceutically acceptable carrier.

Examples of monomers and polymers of the present invention are providedfor some embodiments of the current invention. It can be extended toother species. This selection is not meant to limit the scope of theinvention in any way. Other variations in the procedure may be readilyapparent to those skilled in the art.

EXAMPLE 1 Chloro-acetic acid 2-(2-chloro-acetoxy)-ethyl ester

A solution ethylene glycol (100 grams, 1.611 moles), chloroacetic acid(385 grams, 4.031 moles) and paratoluene sulphonic acid (1 gram) intoluene (750 mL) in a 2 lit 4 neck round bottom flask equipped with amechanical stirrer, Dean-stark apparatus was refluxed for 8 hours,cooled to room temperature. The toluene layer was washed with water(2×300 mL), 5% sodium bicarbonate solution (3×500 mL), water (2×300 mL),dried over sodium sulphate and distilled to get crude 1, which waspurified by high vacuum distillation to get pure 1 (242 grams, 69.8%),which slowly crystallized to white crystals m.p: 44° C., ^(I)H NMR(CDCl₃): δ 4.16 (s, 2H, CH₂), 4.85 (s, 2H, CH₂).

EXAMPLE 2 (4-Methoxycarbonylmethoxy-phenoxy)-acetic acid methyl ester

To a mixture of sodium hydride (60%, 92 grams, 2.3 moles) in DMF (400mL) at 0° C. was carefully added hydroquinone (100 grams, 909 mmol). Themixture was stirred for 30 minutes. Methyl chloro acetate (247 grams,2.276 moles) was added drop wise, and the mixture was stirred at roomtemperature for 2 hours. The reaction mixture was carefully quenchedinto ice water (2 lit). Crude product was filtered, dried, andrecrystallised from a mixture of Ethyl acetate:Hexane (1:6) to give pureproduct (95 grams, 41.1%) as a white powder. M.p: 96-98° C. ^(I)H NMR(CDCl₃) δ 3.68 (s, 3H, Ester), 4.54 (s, 2H₂OCH₂), 6.82 (s, 2H, Ar).

EXAMPLE 3 (4-Carboxymethoxy-phenoxy)-acetic acid

Example 1 (100 grams, 394 mmol) was added to 3.25 M—sodium hydroxidesolution (600 mL). The mixture was heated to 70° C. for 20 hours andpoured onto ice cold water (1 lit) and the pH adjusted to 1 withconcentrated hydrochloric acid. The crude product was filtered, dried,and recrystallised from DMF by precipitating with water to give purecompound (60 grams, 67.4%) as a white powder. Mp: 254-256.5° C. ^(I)HNMR (CDCl₃+DMSO, d₆) 4.44 (s, 2H, OCH₂), 6.72 (s, 2H, Ar).

EXAMPLE 4

To a solution of Example 3 (10 grams, 44.24 mmoles), trietylamine (13.4grams, 132.42 mmoles) in dry dimethylformamide (100 mL) was addedchloroacetic acid 2-(2-chloro-acetoxy)-ethyl ester (9.515 grams, 44.24mmoles), Example 1, and stirred at room temperature for 30 hours. Thesolid triethylamine hydrochloride is filtered and to the filtrate, coldwater (300 mL) was added. The precipitated polymer was filtered,slurried with ethyl acetate, filtered, and dried under vacuum at 50° C.to yield the polymer (10 grams) as a white powder. M.p: 76.5-87° C. Themolecular weights of this polymer was characterized by GPC and theresults are summarized below:

-   Weight-average molecular weight: Mw=16,856-   Number average-average molecular weight: Mn=13,456-   Polydispersity Index (Mw/Mn): P.I=1.25-   z-Average molecular weight: Mz=20,597    Hydrolysis

Polymer 0.5 grams Aldrich pH 9 buffer 50 mL Temperature 100° C.Hydrolyzed in 5 hours

EXAMPLE 5[3-(4-Methoxycarbonylmethoxy-phenyl)-4-oxo-4H-chromen-7-yloxy]-aceticacid methyl ester

To a mixture of Daidzein (20 grams, 79 mmol), anhydrous K₂CO₃ (100grams, 723 mmol), sodium iodide (8 grams, 53.4 mmol), and disodiumphosphate (8 grams, 57 mmol) in anhydrous acetone (600 mL) was addedmethyl chloro acetate (29.2 grams, 269 mmol). The mixture was refluxedfor 6 hours. Acetone was distilled and water (600 mL) added. The crudeproduct was filtered, dried, and recrystallised from toluene to givepure product (22 grams, 70%) as a white powder. M.p: 163-165.7° C.^(I)HNMR (CDCl₃) δ 3.69 (s, 3H, ester), 3.80 (s, 3H, Ester), 4.68 (s,2H, OCH₂), 4.79 (s, 2H, OCH₂), 6.83 (d, 1H, Ar), 6.88 (dd, 2H, B-ring),7.02 (dd, 1H, Ar), 7.46 (dd, 2H, B-ring), 8.00 (s, 1H, pyran), 8.18 (dd,1H, Ar).

EXAMPLE 6 [3-(4-Carboxymethoxy-phenyl)-4-oxo-4H-chromen-7-yloxy]-aceticacid

A mixture of Example 4 (45 grams, 113.5 mmol) and concentrated HCl (250mL) was heated at 90° C. for 5 hours. The reaction mixture was cooled toroom temperature and poured onto ice water (250 mL), filtered, washedwith water and methanol, and dried. The crude product was recrystallisedfrom dimethyl formamide and precipitated with water to give pure product(36 grams, 86.1%) as a white powder. M.p: 270-272.2° C.

EXAMPLE 7

To a solution of Example 6 (10 grams, 27.02 mmoles) and triethylamine(8.20 grams, 81.03 mmoles) in dry dimethylformamide (100 mL) was addedchloroacetic acid 2-(2-chloro-acetoxy)-ethyl ester (5.811 grams, 27.02mmoles), Example 1. The mixture was stirred at room temperature for 30hours. The solid triethylamine hydrochloride was filtered and to thefiltrate, cold water (300 mL) was added. The precipitated polymer wasfiltered, slurried with methanol, filtered, and dried under vacuum at50° C. to get the polymer (11 grams) as white powder. M.p: 80-120° C.The molecular weights of this polymer was characterized by GPC and theresults are summarized below:

-   Weight-average molecular weight: Mw=28,954-   Number average-average molecular weight: Mn=21,238-   Polydispersity Index (Mw/Mn): P.I=1.36-   z-Average molecular weight: Mz=36,256    Hydrolysis

Polymer 0.5 grams Aldrich pH 9 buffer 50 mL Temperature 100° C.Hydrolyzed in 6 hours

EXAMPLE 8

To a solution of terephthallic acid (10 grams, 60.15 mmoles) andtriethylamine (15.3 grams, 151.20 mmoles) in dry dimethylformamide (100mL) was added chloroacetic acid 2-(2-chloro-acetoxy)-ethyl ester (12.94grams, 60.19 mmoles), example 1. The mixture was stirred at roomtemperature for 20 hours. The solid triethylamine hydrochloride isfiltered and to the filtrate, cold water (300 mL) was added. Theprecipitated polymer was filtered slurried with methanol, filtered anddried under vacuum at 50° C. to get polymer 41 (14 grams) as off whitepowder. M.p: 180-189° C.

Hydrolysis

Polymer 0.5 grams Aldrich pH 9 buffer 50 mL Temperature 100° C.Hydrolyzed in 6 hours

EXAMPLE 9 Chloro-acetic acid 4-(2-chloro-acetoxy)-phenyl ester

A mixture of hydroquinone (50 grams, 454.09 mmol) and chloroacetylchloride (150 mL) was refluxed for 48 hours. Excess chloroacetylchloride was distilled off, and the residue taken into ice water,filtered, dried, and recrystallised from ethyl acetate:hexane (1:6) toget pure product (55 grams, 46%) as a white fluffy powder. M.p: 127-128°C. ¹H NMR (CDCl₃) δ 4.20 (s, 25H, CH₂), 7.24 (s, 2H, Ar).

EXAMPLE 10

To a mixture of Example 3 (8.6 grams, 38.02 mmol) and triethylamine(13.43 grams, 132.72 mmol) in dry dimethyl formamide (100 mL) was addedchloroacetic acid 4-(2-chloro-acetoxy)-phenyl ester (10 grams, 38.01mmol), Example 9. The mixture was stirred at room temperature for 48hours. The solid triethylamine hydrochloride was filtered off, and theDMF solution was taken into ice water, filtered, dried, slurried inmethanol followed by ethyl acetate, and dried under vacuum to get purepolymer (13 grams) as a white powder. M.p: 232-234° C.

EXAMPLE-11 {2-[4-(2-Carboxymethoxy-ethoxy)-phenoxy]-ethoxy}-acetic acid

To a suspension of sodium hydride (60%, 132 grams, 3.30 moles) inanhydrous dimethyl formamide (600 mL) under nitrogen atmosphere at 0° C.was added Hydroquinone bis ethanol (150 grams, 756.7 mmoles) in smalllots, later stirred at room temperature for one hour. To the abovemixture was added a solution of chloroacetic acid (195 grams, 2.06moles) in anhydrous Dimethyl formamide (300 mL) very cautiously dropwise as the reaction is exothermic. Later the reaction is maintained at800° C. for one hour and left at room temperature for 16 hours. Reactionmixture carefully poured onto ice (3 kg), extracted with Ethyl acetate(2×500 mL) and organic phase discarded. The aqueous layer pH is adjustedto 2 with 3N-Hydrochloric acid and extracted into ethyl acetate. Theethyl acetate extract was washed with 5% sodium bicarbonate (4×75 mL).The ethyl acetate layer discarded. The aqueous layer washed with ethylacetate (3×200 mL), acidified with concentrate HCl to pH-2, extractedwith ethyl acetate, dried over sodium sulphate, distilled, andprecipitated with hexane (500 mL) to get pure 1 (75 grams, 39.6%) as anoff white powder. M.p: 112-115.5° C. ¹H NMR (CDCl₃) δ 3.84 (m, 2H, CH₂),4.06 (m, 4H, CH₂x₂), 6.82 (s, 2H, Ar).

EXAMPLE 12 Polymer of{2-[4-(2-Carboxymethoxy-ethoxy)-phenoxy]-ethoxy}-acetic acid

To a mixture of {2-[4-(2-Carboxymethoxy-ethoxy)-phenoxy]-ethoxy}-aceticacid (10 grams, 31.817 mmol) and Example 11, triethylamine (9.656 grams,95.424 mmol) in dry dimethylformamide (100 mL) was added Example 1 (6.84grams, 31.81 mmol). The mixture was stirred at room temperature for 96hours. The solid triethylamine hydrochloride was filtered off and washedwith DMF, and the solvent was distilled off under vacuum. The polymerwas washed with isopropyl alcohol (6×35 mL) and dried using a highvacuum pump at 40° C. for 4 hours to recover and amber colored viscoussyrup.

When ranges are used herein for physical properties, such as molecularweight, or chemical properties, such as chemical formulae, allcombinations and subcombinations of ranges and specific embodimentstherein are intended to be included.

The disclosures of each patent, patent application and publication citedor described in this document are hereby incorporated herein byreference, in their entirety.

Those skilled in the art will appreciate that numerous changes andmodifications can be made to the preferred embodiments of the inventionand that such changes and modifications can be made without departingfrom the spirit of the invention. It is, therefore, intended that theappended claims cover all such equivalent variations as fall within thetrue spirit and scope of the invention.

[Embodiment 1] A biodegradable polyester of formula III, VI, or XI, or abiodegradable polyamide ester of formula VIII or IX, or apharmaceutically acceptable salt thereof:

(A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III

wherein the polyester of formula III is formed by condensationpolymerization of monomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II

(B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VI

-   -   wherein the polyester of formula IV is formed by condensation        polymerization of monomers of formula IV and V:        R₆(Y²)_(a)—R₅—(X²)_(b)—R₇  IV        H—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V

(C)—[(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(o)—  VIII

-   -   wherein the polyamide ester of formula VIII is formed by        condensation polymerization of monomers of formula Va and VII:        H—(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—H  Va        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

(D)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(p)—  IX

-   -   wherein the polyamide ester of formula IX is formed by        condensation polymerization of monomers of formula I and VII:        H—(X)_(a)—O—R₁—O—(Y)_(b)—H  I        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

(E)[—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—]—  XIwherein the polyester of formula XI is formed by self condensationpolymerization of a monomer of formula X:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X

wherein:

-   -   m, n, o, p, and q are each independently an integer from about 5        to about 1000;    -   R₁, R₅, R₉, and R₁₃ are each independently the remaining portion        of a biologically active compound;    -   R₂, R₈, and R₁₀ are each independently the remaining portion of        a biologically active compound or non-biologically active        compound;    -   R₃, R₄, R₆, R₇, R₁₁, R₁₂, and R₁₃ are each independently        selected from Cl, F, Br, and I;    -   X, X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y, Y¹, and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24;    -   each a, b, c, and d is independently an integer from about 1 to        about 6;    -   each e is independently an integer from about 1 to about 6; and    -   each f is independently an integer from about 0 to about 6.

[Embodiment 2] A biodegradable polyester of Embodiment 1 having formulaIII or a pharmaceutically acceptable salt thereof:—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III

wherein the polyester is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II

wherein:

-   -   m is an integer from about 5 to about 1000;    -   R₁ is the remaining portion of a biologically active compound;    -   R₂ is the remaining portion of a biologically active compound or        non-biologically active compound;    -   R₃ and R₄ are independently selected from Cl, F, Br, and I;    -   X and X¹ are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y and Y¹ are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

[Embodiment 3] A biodegradable polyester of Embodiment 1 having formulaVI or a pharmaceutically acceptable salt thereof:—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VI

-   -   wherein the polyester is formed by condensation polymerization        of monomers of formula IV and V:        R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IV        H—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V

wherein:

-   -   n is an integer from about 5 to about 1000;    -   R₅ is the remaining portion of a biologically active compound;    -   R₆ and R₇ are independently selected from Cl, F, Br, and I;    -   R₈ is the remaining portion of a biologically active compound or        non-biologically active compound;    -   X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y¹ and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O-(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

[Embodiment 4] A biodegradable polyamide ester of Embodiment 1 havingformula VIII or a pharmaceutically acceptable salt thereof:—[(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(o)—  VIII

-   -   wherein the polyamide ester is formed by condensation        polymerization of monomers of formula Va and VII:        H—(X¹)_(c)—O(O═)C—R₉—C(═O)O—(Y¹)_(d)—H  Va        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

wherein:

-   -   o is an integer from about 5 to about 1000;    -   R₉ is the remaining portion of a biologically active compound;    -   R₁₀ is the remaining portion of a biologically active compound        or non-biologically active compound;    -   R₁₁ and R₁₂ are independently selected from Cl, F, Br, and I;    -   X¹ and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—;    -   Y¹ and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

[Embodiment 5] A biodegradable polyamide ester of Embodiment 1 havingformula IX or a pharmaceutically acceptable salt thereof:—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)]_(p)—  IX

-   -   wherein the polyamide ester is formed by condensation        polymerization of monomers of formula I and VII:        H—(X)_(a)—O—R₁—O—(Y)_(b)—H  I        R₁₁—(Y²)_(a)—CH₂(O═)C—NH—R₁₀—NH—C(═O)CH₂—(X²)_(b)—R₁₂  VII

wherein:

-   -   p is an integer from about 5 to about 1000;    -   R₁ is the remaining portion of a biologically active compound;    -   R₁₀ is the remaining portion of a biologically active compound        or non-biologically active compound;    -   R₁₁ and R₁₂ are independently selected from Cl, F, Br, and I;    -   X and X² are independently at each occurrence —OC(═O)CH₂—        (inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic        acid moiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid        moiety), —OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid        moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—; and,    -   Y and Y² are independently at each occurrence —CH₂C(═O)O—        (glycolic acid moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each y and z is independently an integer from about 2 to about        24; and    -   each a, b, c, and d is independently an integer from about 1 to        about 6.

[Embodiment 6] A biodegradable polyester of Embodiment 1 having formulaXI or a pharmaceutically acceptable salt thereof:[—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—]_(q)—  XI

-   -   wherein the polyester is formed by self condensation        polymerization of a monomer of formula X:        R₁₄—(X)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X        wherein:    -   q is an integer from about 5 to about 1000;    -   R₁₃ is the remaining portion of a biologically active compound;    -   R₁₄ is selected from Cl, F, Br, and I;    -   Y is independently at each occurrence —CH₂C(═O)O— (glycolic acid        moiety), —CH(CH₃)C(═O)O— (lactic acid moiety),        —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O—        (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or        —(CH₂CH₂O)_(z)CH₂C(═O)O—;    -   each e is independently an integer from about 1 to about 6; and    -   each f is independently an integer from about 0 to about 6.

[Embodiment 7] A polyester of Embodiment 3, wherein the non-biologicallyactive compound is a dicarboxylic compound selected from:

[Embodiment 8] A polyester of Embodiment 2, wherein the non-biologicallyactive compound is a diamino compound selected from:

[Embodiment 9] A polyamide ester of Embodiment 4, wherein thenon-biologically active compound is a diamino compound selected from:

[Embodiment 10] A polyamide ester of Embodiment 5, wherein thenon-biologically active compound is a diamino compound selected from:

[Embodiment 11] A biodegradable monomer of Embodiment 1, which isselected from a monomer of formula I, II, IV, V, Va, VII, and X.

[Embodiment 12] A composition comprising at least two differentpolymers, wherein each polymer is independently a polymer according toEmbodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 13] A cosmetic composition comprising a cosmetic ingredientand at least one polymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8,9, or 10.

[Embodiment 14] An implantable medical device comprising at least onepolymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 15] An implantable medical device of Embodiment 14, whereinthe polymer has been further polymerized with a lactone monomer selectedfrom glycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.

[Embodiment 16] An implantable medical device of Embodiment 14, whereinthe device is a stent.

[Embodiment 17] An implantable medical device of Embodiment 16, whereinthe polymer has been further polymerized with a lactone monomer selectedfrom glycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.

[Embodiment 18] An implantable medical device of Embodiment 14, whereinthe device is a scaffold for tissue engineer, comprising a porousstructure for the attachment and proliferation of cells.

[Embodiment 19] An implantable medical device of Embodiment 18, whereinthe polymer has been further polymerized with a lactone monomer selectedfrom glycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.

[Embodiment 20] A coating for a stent comprising at least one polymeraccording to Embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 21] A stent coating of Embodiment 20, wherein the polymerhas been further polymerized with a lactone monomer selected fromglycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.

[Embodiment 22] A drug delivery system comprising at least one polymeraccording to Embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 physicallyadmixed with a biologically or pharmacologically active agent.

[Embodiment 23] A drug delivery system wherein the biologically orpharmacologically active agent is physically embedded or dispersed intothe polymer and the polymer is in the form of a polymeric matrix.

[Embodiment 24] A suture coating comprising at least one polymeraccording to Embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 25] A suture comprising at least one polymer according toEmbodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 26] An antimicrobial agent comprising at least one polymeraccording to Embodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 27] A method for treating a disease in a patient comprisingadministering to an animal in need of such therapy, an effective amountof at least one polymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8,9, or 10.

[Embodiment 28] A method for producing an analgesic effect in a patient,comprising administering to an animal in need of such therapy, aneffective amount of at least one polymer according to Embodiment 1, 2,3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 29] A method for treating cancer in a patient comprisingadministering to an animal in need of such therapy, an effective amountof at least one polymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8,9, or 10.

[Embodiment 30] A method for producing an anti-inflammatory effect in apatient comprising administering to an animal in need of such therapy,an effective amount of at least one polymer according to Embodiment 1,2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 31] A method for producing an anti-bacterial effect in apatient comprising administering to an animal in need of such therapy,an effective amount of at least one polymer according to Embodiment 1,2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 32] A method for producing an anti-fungal effect in apatient comprising administering to an animal in need of such therapy,an effective amount of at least one polymer according to Embodiment 1,2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 33] A therapeutic method for producing an immunosuppressiveeffect in a patient comprising administering to an animal in need ofsuch therapy, an effective amount of at least one polymer according toEmbodiment 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 34] A method for producing an anti-thrombotic effect in anpatient comprising administering to an animal in need of such therapy,an effective amount of at least one polymer according to Embodiment 1,2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 35] A method for treating psoriasis, inflammatory boweldisease, skin cancer, or a brain tumor in an patient, comprisingadministering to an animal in need of such therapy, an effective amountof at least one polymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8,9, or 10.

[Embodiment 36] A method for producing an anti-infective effect in apatient, comprising administering to an animal in need of such therapy,an effective amount of at least one polymer according to Embodiment 1,2, 3, 4, 5, 6, 7, 8, 9, or 10.

[Embodiment 37] A method for treating pain in a patient, comprisingadministering to an animal in need of such therapy, an effective amountof at least one polymer according to Embodiment 1, 2, 3, 4, 5, 6, 7, 8,9, or 10.

What is claimed is:
 1. A composition comprising at least two differentpolymers, wherein each polymer is independently selected from: abiodegradable polyester of formula III, VI, or XI, or a pharmaceuticallyacceptable salt thereof: (A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II B—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independently the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄, R₆, R₇, and R₁₄ are each independently selected from Cl, F, Br, andI; X, X¹, and X² are independently at each occurrence —OC(═O)CH₂—(inverse glycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic acidmoiety), —OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety), —OC(═O)(CH₂)_(y)—, or —OC(═O)(OCH₂CH₂)_(z)—: Y, Y¹, and Y² are independently ateach occurrence —CH₂C(═O)O— (glycolic acid moiety), —CH(CH₃)C(═O)O—(lactic acid moiety), —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety),—CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety), —(CH₂ )_(y)C(═O)O—, or—(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z is independently an integer fromabout 2 to about 24; each a, b, c, and d is independently an integerfrom about 1 to about 6; each e is independently an integer from about 1to about 6; and each f is independently an integer from about 0 to about6.
 2. A cosmetic composition comprising a cosmetic ingredient and atleast one polymer selected from: a biodegradable polyester of formulaIII, VI, or XI, or a pharmaceutically acceptable salt thereof: (A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R_(5—(X) ²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄, R₆, R₇, and R₁₄ are each independent selected from Cl, F, Br, and I:X, X¹, and X² are independent at each occurrence —OC(═O)CH₂— (inverseglycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety),—OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂— (OCH₂CH₂)_(z)—; Y, Y¹, and Y² areindependently at each occurrence —CH₂C(═O)O— (glycolic acid moiety),—CH(CH₃)C(═O)O— (lactic acid moiety), —CH₂CH₂OCH₂C(═O)O— (dioxanonemoiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety),—(CH₂)_(y)C(═O)O—, or —(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z isindependently an integer from about 2 to about 24; each a, b, c, and dis independently an integer from about 1 to about 6; each e isindependently an integer from about 1 to about 6; and each f isindependently an integer from about 0 to about
 6. 3. An implantablemedical device or coating, comprising at least one polymer selectedfrom: a biodegradable polyester of formula III, VI, or XI, or apharmaceutically acceptable salt thereof: (A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹ _(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d]) _(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the portion of a biologicallyactive compound or non-biologically active compound; R₃, R₄, R₆, R₇, andR₁₄ are each independent selected from Cl, F, Br, and I; X, X¹, and X²are independent at each occurrence —OC(═O)CH₂— (inverse glycolic acidmoiety), —OC(═O)CH(CH₃)— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety), —OC(═O)CH₂CH ₂CH₂CH₂CH₂— (inverse caprolactone acid moiety), —OC(═O)(CH₂)_(y)—, or—OC(═O)CH₂(OCH₂CH₂)_(z)—; Y, Y¹, and Y² are independently at eachoccurrence —CH₂C(═O)O— (glycolic acid moiety), —CH(CH₃)C(═O)O— (lacticacid moiety), —CH₂CH₂OCH₂C(═O)O— (dioxanone moiety),—CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety), —(CH₂)_(y)C(═O)O—, or—(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z is independently an integer fromabout 2 to about 24; each a, b, c, and d is independently an integerfrom about 1 to about 6; each e is independently an integer from about 1to about 6; and each f is independently an integer from about 0 to about6.
 4. An implantable medical device or coating of claim 3, wherein thepolymer has been further polymerized with a lactone monomer selectedfrom glycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.
 5. An implantable medicaldevice or coating of claim 3, wherein the device is a stent.
 6. Animplantable medical device or coating of claim 5, wherein the polymerhas been further polymerized with a lactone monomer selected fromglycolide, lactide, ε-caprolactone, trimethylene carbonate, etherlactones, morpholinediones, and p-dioxanone.
 7. An implantable medicaldevice or coating of claim 3, wherein the device is a scaffold fortissue engineer comprising a porous structure for the attachment andproliferation of cells.
 8. An implantable medical device or coating ofclaim 7, wherein the polymer has been further polymerized with a lactonemonomer selected from glycolide, lactide, ε-caprolactone, trimethylenecarbonate, ether lactones, morpholinediones, and p-dioxanone.
 9. Animplantable medical device or coating of claim 3, wherein the device isa coating for a stent.
 10. An implantable medical device or coating ofclaim 9, wherein the polymer has been further polymerized with a lactonemonomer selected from glycolide, lactide, ε-caprolactone, trimethylenecarbonate, ether lactones, morpholinediones, and p-dioxanone.
 11. Animplantable medical device or coating of claim 3, wherein the coating isa suture coating.
 12. An implantable medical device or coating of claim3, wherein the device is a suture.
 13. An implantable medical device orcoating of claim 3, wherein the polymer is a biodegradable polyesterhaving formula III or a pharmaceutically acceptable salt thereof:—[(X)_(a)—O—R₁—O—(Y)^(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III.
 14. Animplantable medical device or coating of claim 3, wherein the polymer isa biodegradable polyester having formula VI or a pharmaceuticallyacceptable salt thereof:—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VI. 15.An implantable medical device or coating of claim 3, wherein the polymeris a biodegradable polyester having formula XI or a pharmaceuticallyacceptable salt thereof:—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI.
 16. An implantable medicaldevice or coating of claim 3, wherein the polymer is a biodegradablepolyester of claim 14, wherein the non-biologically active compound is adicarboxylic compound selected from:


17. A drug delivery system comprising at least one polymer according toclaim 1 physically admixed with a biologically or pharmacologicallyactive agent, wherein the polymer is selected from: a biodegradablepolyester of formula III, VI, or XI, or a pharmaceutically acceptablesalt thereof: (A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈ 13 C(═O)O—(Y¹)_(d)]_(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃ —C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄,R₆, R₇, and R₁₄ are each independent selected from Cl, F, Br, and I; X,X¹, and X² are independent at each occurrence —OC(═O)CH₂— (inverseglycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety),—OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂ )_(z)—; Y, Y¹, and Y² areindependently at each occurrence —CH₂C(═O)O— (glycolic acid moiety),—CH(CH₃)C(═O)O— (inverse lactic acid moiety), —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety),—(CH₂)_(y)C(═O)O—, or —(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z isindependently an integer from about 2 to about 24; each a, b, c, and dis independently an integer from about 1 to about 6; each e isindependently an integer from about 1 to about 6; and each f isindependently an integer from about 0 to about
 6. 18. A drug deliverysystem of claim 17, wherein the biologically or pharmacologically activeagent is physically embedded or dispersed into the polymer and thepolymer is in the form of a polymeric matrix.
 19. An antimicrobial agentcomprising at least one polymer selected from: a biodegradable polyesterof formula III, VI, or XI, or a pharmaceutically acceptable saltthereof: (A)—[(X)_(a)—O—R₁—O—(Y)^(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄, R₆, R₇, and R₁₄ are each independent selected from Cl, F, Br, and I;X, X¹, and X² are independent at each occurrence —OC(═O)CH₂— (inverseglycolic acid moiety), —CH(CH₃)C(═O)O— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety),—OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—; Y, Y¹, and Y² areindependently at each occurrence —CH₂C(═O)O— (glycolic acidmoiety),—CH(CH₃)C(═O)O— (lactic acid moiety), —CH₂CH₂OCH₂C(═O)O—(dioxanone moiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety),—(CH₂)_(y)C(═O)O—, or —(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z isindependently an integer from about 2 to about 24; each a, b, c, and dis independently an integer from about 1 to about 6; each e isindependently an integer from about 1 to about 6; and each f isindependently an integer from about 0 to about
 6. 20. A method fortreating a disease in a patient, comprising administering to an animalin need of such therapy, an effective amount of at least one polymerselected from: a biodegradable polyester of formula III, VI, or XI, or apharmaceutically acceptable salt thereof: (A)—[(X)_(a)—O—R₁—O—(Y)_(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)O—(Y¹)_(d)]_(n)—  VI wherein thepolyester of formula IV is formed by condensation polymerization ofmonomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄, R₆, R₇, and R₁₄ are each independently selected from Cl, F, Br, andI; X, X¹, and X² are independent at each occurrence —OC(═O)CH₂— (inverseglycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety),—OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂)_(z)—; Y, Y¹, and Y² areindependently at each occurrence —CH₂C(═O)O— (glycolic acid moiety),—CH(CH₃)C(═O)O— (lactic acid moiety), —CH₂CH₂OCH₂C(═O)O— (dioxanonemoiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety),—(CH₂)_(y)C(═O)O—, or —(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z isindependently an integer from about 2 to about 24; each a, b, c, and dis independently an integer from about 1 to about 6; each e isindependently an integer from about 1 to about 6; and each f isindependently an integer from about 0 to about
 6. 21. A method of claim20, wherein the disease is cancer.
 22. A method of claim 20, wherein thedisease is selected from psoriasis, inflammatory bowel disease, skincancer, and a brain tumor.
 23. A method for producing an effect in apatient comprising administering to an animal in need of such therapy,an effective amount of at least one polymer selected from: abiodegradable polyester of formula III, VI, or XI, or a pharmaceuticallyacceptable salt thereof and the effect being selected from an analgesiceffect, anti-inflammatory effect, anti-bacterial effect, an anti-fungaleffect, an immunosuppressive effect, an anti-thrombotic effect, and ananti-infective effect, wherein: (A)—[(X)_(a)—O—R₁—O—(Y)^(b)—(Y¹)_(c)—R₂—(X¹)_(d)]_(m)—  III wherein thepolyester of formula III is formed by condensation polymerization ofmonomers of formula I and II:H—(X)_(a)—O—R₁—O—(Y)_(b)—H  IR₃—(Y¹)_(c)—R₂—(X¹)_(d)—R₄  II (B)—[(Y²)_(a)—R₅—(X²)_(b)—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)]_(n)—  VIwherein the polyester of formula IV is formed by condensationpolymerization of monomers of formula IV and V:R₆—(Y²)_(a)—R₅—(X²)_(b)—R₇  IVH—(X¹)_(c)—O(O═)C—R₈—C(═O)O—(Y¹)_(d)—H  V (E)—[(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)]_(g)—  XI wherein the polyester of formulaXI is formed by self condensation polymerization of a monomer of formulaX:R₁₄—(Y)_(e)—R₁₃—C(═O)O—(Y)_(f)—H  X wherein: m, n, and q are eachindependently an integer from about 5 to about 1000; R₁, R₅, and R₁₃ areeach independent the remaining portion of a biologically activecompound; R₂ and R₈ are each independently the remaining portion of abiologically active compound or non-biologically active compound; R₃,R₄, R₆, R₇, and R₁₄ are each independent selected from Cl, F, Br, and I;X, X¹, and X² are independently at each occurrence —OC(═O)CH₂— (inverseglycolic acid moiety), —OC(═O)CH(CH₃)— (inverse lactic acid moiety),—OC(═O)CH₂OCH₂CH₂— (inverse dioxanone acid moiety),—OC(═O)CH₂CH₂CH₂CH₂CH₂— (inverse caprolactone acid moiety),—OC(═O)(CH₂)_(y)—, or —OC(═O)CH₂(OCH₂CH₂ )_(z)—; Y, Y¹, and Y² areindependently at each occurrence —CH₂C(═O)O— (glycolic acid moiety),—CH(CH₃)C(═O)O— (lactic acid moiety), —CH₂CH₂OCH₂C(═O)O— (dioxanonemoiety), —CH₂CH₂CH₂CH₂CH₂C(═O)O— (caprolactone moiety),—(CH₂)_(y)C(═O)O—, or —(CH₂CH₂O)_(z)CH₂C(═O)O—; each y and z isindependently an integer from about 2 to about 24; each a, b, c, and dis independently an integer from about 1 to about 6; each e isindependently an integer from about 1 to about 6; and each f isindependently an integer from about 0 to about
 6. 24. A method of claim23, wherein the effect is an anti-inflammatory effect.
 25. A method ofclaim 23, wherein the effect is an anti-bacterial effect.
 26. A methodof claim 23, wherein the effect is an anti-fungal effect.
 27. A methodof claim 23, wherein the effect is an immunosuppressive effect.
 28. Amethod of claim 23, wherein the effect is an anti-thrombotic effect. 29.A method of claim 23, wherein the effect is an anti-infective effect.30. A method of claim 23, wherein the effect is an analgesic effect.